- --------------------------------------------------------------------------------
                       SECURITIES AND EXCHANGE COMMISSION

                             Washington, D.C. 20549
- --------------------------------------------------------------------------------



                                   FORM 8-K/A

                    PURSUANT TO SECTION 13 OR 15 (d) OF THE
                        SECURITIES EXCHANGE ACT OF 1934


       Date of Report (Date of earliest event reported) October 18, 1995
             Amendment Number 1 to Form 8-K filed October 21, 1995


                               CONMED CORPORATION

             (Exact name of registrant as specified in its charter)


           New York                      0-16093                 16-0977505
- -------------------------------        -----------           -------------------
(State or other jurisdiction of        (Commission           (I.R.S. Employer
incorporation or organization)         File Number)          Identification No.)

   310 Broad Street, Utica, New York                             13501
- ----------------------------------------                       ----------
(Address of principal executive offices)                       (Zip Code)


                                 (315) 797-8375
              ----------------------------------------------------
              (Registrant's telephone number, including area code)

                                      N/A
         -------------------------------------------------------------
         (Former name or former address, if changes since last report)


Item 5.  Other Events

                  On October 18, 1995, CONMED  Corporation and New Dimensions in
Medicine,  Inc. (NDM)  announced the signing of an asset  purchase  agreement in
which  CONMED will acquire  substantially  all of the business and assets of NDM
except for NDM's international wound care business, for a cash purchase price of
approximately  $32,000,000.  The  transaction  is  subject  standard  government
approvals and the approval of the shareholders of NDM. Subject to receiving such
approvals,  the parties  expect the  transaction  to close the first  quarter in
1996.


Item 7. Financial Statements and Exhibits

        (c) Exhibits

            1.  Consolidated  Financial  Statement of MEI  Diversified  Inc. and
Subsidiaries  as of October  14, 1994 and  December  31,  1993,  and the related
consolidated  statements of operations,  stockholders' equity (deficit) and cash
flows for the period ended October 14, 1994 and for each of the two years in the
period ended December 31, 1993.

            2. Consolidated  Financial  Statement of New Dimensions in Medicine,
Inc. and  Subsidiaries  as of December  31, 1994 and October 15,  1994,  and the
related consolidated  statements of income,  stockholders' equity and cash flows
for the ten week period ended December 31, 1994.

            3. Consolidated  Financial  Statement of New Dimensions in Medicine,
Inc. and  Subsidiaries  as of September 30, 1995,  and the related  consolidated
statements  of income and cash flows for the nine  months  ended  September  30,
1995.

                                   SIGNATURE


         Pursuant to the  requirements  of the Securities  Exchange Act of 1934,
the  Registrant  has duly  caused  this report to be signed on its behalf by the
undersigned thereunto duly authorized.



                                               CONMED CORPORATION



                                               By: /s/ Robert D. Shallish, Jr.
                                                   Vice President-Finance


Dated:  December 21, 1995

                       SECURITIES AND EXCHANGE COMMISSION
                             Washington, D.C. 20549

                             FORM 10-K (As Amended)

           [X]      ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF
                    THE SECURITIES EXCHANGE ACT OF 1934

For the Year Ended December 31, 1994                 Commission File No. 1-09156

           [  ]     TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF
                    THE SECURITIES EXCHANGE ACT OF 1934


                        NEW DIMENSIONS IN MEDICINE, INC.
             (Exact name of registrant as specified in its charter)

                                    Delaware
                        (State or other jurisdiction of
                         incorporation or organization)

                                   41-1549475
                                (I.R.S. Employer
                              Identification No.)

                    3040 East River Road, Dayton, Ohio 45439
              (Address of principal executive offices) (Zip code)

       Registrant's telephone number, including area code: (513) 294-1767

Securities registered pursuant to Section 12(b) of the Act:

                                      None

          Securities registered pursuant to Section 12(g) of the Act:

                          Common Stock, $.01 par value

     Indicate  by check mark  whether the  registrant  (1) has filed all reports
required to be filed by Section 13 or 15(d) of the  Securities  Exchange  Act of
1934  during  the  preceding  12 months  (or for such  shorter  period  that the
registrant was required to file such reports),  and (2) has been subject to such
filing requirements for the past 90 days. YES [ X ]    NO [   ]

     Indicate by check mark if disclosure of delinquent  filers pursuant to Item
405 of Regulation S-K is not contained herein, and will not be contained, to the
best  of  the  registrant's   knowledge,  in  definitive  proxy  or  information
statements  incorporated  by  reference  in Part  III of this  Form  10-K or any
amendment to this Form 10-K. [  ]

     As of March 31, 1995,  4,311,977  shares of Common Stock of the  registrant
were outstanding, approximately 1,690,833 shares of which are beneficially owned
by  affiliates  of the  registrant.  There  is no  established  trading  market.
Pursuant  to a plan of  reorganization,  the  registrant  intends  to  submit an
application  for  inclusion of the Common Stock on the National  Association  of
Securities    Dealers    Automated    Quotation     ("NASDAQ")    System.    See
"BUSINESS-Background."  However, there can be no assurance that such application
will be approved, and until such time the registrant expects the Common Stock to
be traded on local over-the-counter markets.

     Indicate by check mark whether the  registrant  has filed all documents and
reports  required  to be  filed by  Section  12,  13 or 15(d) of the  Securities
Exchange Act of 1934 subsequent to the  distribution of securities  under a plan
confirmed by a court. YES [ X ]    NO [   ]

                                     PART I

Item 1.   BUSINESS.

Background

         New  Dimensions  In Medicine,  Inc. (the  "Company" or "NDM")  designs,
develops,  manufactures  and markets a broad line of specialty  medical products
through its Patient  Care  Division and its Critical  Care  Division.  While the
substantial  majority of the  Company's  revenues  are  currently  generated  by
critical care  products,  the Company  expects sales of patient care products to
grow at a higher rate than critical  care  products.  NDM's  strategy for future
growth is to use its base of  proprietary  technology  as a platform  to develop
customer-driven,  specialty  medical  products,  primarily  for the treatment of
chronic wounds and  prevention of deep vein  thrombosis.  The Company  initially
developed its  proprietary  hydrogel as a conductor for its  electrodes  and now
uses it in its  ClearSite(R)  hydrogel  wound care  dressings,  as an  occlusive
dressing to treat chronic wounds and ulcers.

         NDM's Patient Care Division  consists of  ClearSite(R)  hydrogel  wound
care dressings and the Act One(TM) Foot Pump. ClearSite hydrogel wound dressings
are based on proprietary technology designed to treat chronic wounds and ulcers.
NDM  produces  ClearSite  in a number of sizes and forms for use in a variety of
applications,  depending on the type of wound, the location of the wound and the
patient.  The Act One Foot Pump is a foot  compression  device  consisting  of a
slipper for the patient's  foot and a pump which  inflates the slipper.  The Act
One is designed to treat chronic  wound  conditions,  such as the  prevention of
venous  stasis,  reduction of chronic leg ulcers and reduction of leg pain.  The
Act One Foot Pump is also used as a  prophylactic  device to  prevent  deep vein
thrombosis.  NDM's  Critical Care Division  consists of  electrodes,  cables and
wires and  electrosurgical  products.  NDM sells  various  types of  monitoring,
resting,  stress and specialty electrodes,  as well as cables and wires designed
to connect the patient to the monitor.  NDM's  electrosurgical  products include
two  types  of  electrosurgical  grounding  pads,  pencils,  the  PowerPoint(TM)
generator and Endoflex(TM)  flexible  retractors for minimally invasive surgery.
One  line of  NDM's  grounding  pads  uses the  Company's  proprietary  hydrogel
technology.

         As used in this Annual  Report,  the terms  "Company" or "NDM" refer to
New  Dimensions In Medicine,  Inc., a Delaware  corporation.  The Company is the
surviving entity of the merger of NDM Acquisition Corp., a Minnesota corporation
("Old  NDM"),   into  MEI  Diversified   Inc.,  a  Delaware   corporation  ("MEI
Diversified").  In  connection  with the merger,  MEI  Diversified  restated its
Certificate  of  Incorporation  and  changed  its  name  to "New  Dimensions  In
Medicine,  Inc."  The  merger  was  completed  as  part of the  Amended  Plan of
Reorganization  of  the  Official  Committee  of  Unsecured  Creditors  for  MEI
Diversified,   et.  al.,   dated  as  of  September   27,  1994  (the  "Plan  of
Reorganization").  On September 28, 1994, the U.S.  Bankruptcy  Court entered an
order confirming the Plan of Reorganization,  and it became effective on October
14, 1994.  Pursuant to the Plan of Reorganization (a) the executive officers and
Board of Directors of MEI Diversified were removed,  (b) the executive  officers
of Old NDM became the executive  officers of NDM and (c) and new directors  were
elected to the  Company's  Board of  Directors.  See  "Directors  and  Executive
Officers." The Company has abandoned the strategy of being a diversified holding
company  adopted by the  former  management  of MEI  Diversified.  Instead,  the
Company is continuing the medical products business,  as discussed above, of Old
NDM, formerly operated as a subsidiary of MEI Diversified.

         As of March 31, 1995,  a total of  4,311,977  shares of Common Stock of
NDM have been issued to certain  creditors  of MEI  Diversified,  including  the
holders of the 12-1/2% Senior Subordinated Notes of MEI Diversified due December
1, 1996 in the original  principal  amount of $75,000,000 and the 8% Convertible
Debentures  of MEI  Diversified  due December 1, 2006 in the original  principal
amount of $50,000,000 in partial  satisfaction of their claims. The Company will
issue a total of 4,500,000  shares of Common Stock to such creditors  initially.
As of March 31, 1995,  4,311,977 shares of Common Stock have been issued to such
creditors.  A total of  500,000  shares of Common  Stock  will be  reserved  for
issuance  to  satisfy  claims  being  made by certain  former  creditors  of MEI
Diversified  to which  the  trust  administrator  established  under the Plan of
Reorganization  is  objecting.  To the  extent  that these  claims  are  denied,
additional shares of Common Stock will not be issued.  The allowed claim of each
such  creditor  of MEI  Diversified  will be  reduced by $7.60 for each share of
Common Stock of NDM distributed to such creditors.  Effective  October 14, 1994,
all  assets and  liabilities  of MEI  Diversified  were  distributed  to certain
liquidating  estates  established under the Plan of  Reorganization,  except for
certain  tax  attributes  of MEI  Diversified,  the  capital  stock  of  certain
nonoperating subsidiaries and the capital stock of Old NDM. Accordingly,  NDM is
not responsible  for any of the  liabilities or obligations of MEI  Diversified.
The tax attributes of MEI Diversified  and its  nonoperating  subsidiaries  were
retained by NDM in order to preserve  certain net operating  loss  carryforwards
generated  by MEI  Diversified.  As a  result  of the  merger,  all  assets  and
liabilities of Old NDM became assets and liabilities of the Company, except that
all  liabilities  of  Old  NDM  to MEI  Diversified  or  any  of its  affiliates
(including  indebtedness  of  approximately  $22,916,000 as of October 14, 1994)
were cancelled pursuant to the Plan of Reorganization.

Products

         Patient Care Division

         NDM's patient care division  consists of ClearSite  hydrogel wound care
dressings and the Act One Foot Pump.  Management  believes that the patient care
products  are  NDM's  most  important  products  for the  future  and  represent
significant growth opportunities for NDM.

         Specialty  wound care dressings,  such as ClearSite,  are used to treat
chronic  conditions,  such as chronic venous ulcers,  chronic  pressure  ulcers,
diabetic ulcers,  stump sores and skin diseases,  and acute conditions,  such as
surgical  incisions  and burns.  It is estimated  that between 1.5 and 4 million
people  suffer  from  chronic  non-healing  wounds in the United  States.  It is
estimated that the specialty wound care dressing market was  approximately  $350
million in 1992.

         NDM has developed a proprietary hydrogel technology, which it currently
manufactures  and markets under the name ClearSite.  Hydrogels are prepared from
water  insoluble  polymers that can be formulated to produce water absorbent gel
matrices.  Hydrogels  are  often  used  in  medical  applications  because  they
generally have  excellent  biocompatibility  characteristics.  NDM's hydrogel is
also cross-linked,  which provides several significant advantages resulting from
the fact that cross-  linked  hydrogels  can be  manufactured  in sheet form. In
sheet form,  hydrogels,  like ClearSite,  are transparent,  soft, conform to the
skin,  provide a  cushion  to the skin and can be cut to  shape.  NDM  initially
developed its proprietary hydrogel technology to improve its electrode products,
and NDM uses its  hydrogel in its newest  electrodes,  as well as its  grounding
pads.

         ClearSite is a completely  transparent  wound dressing that consists of
hydrogel  and  a  flexible,   continuous  polyurethane  film  covering.  Because
ClearSite is transparent, the health care provider is able to monitor the course
of healing without removing the wound dressing.  ClearSite absorbs wound exudate
and,  as the  gel  begins  to  saturate,  moisture  vapor  transpires  into  the
atmosphere. This cycle continues throughout the healing process to help maintain
balanced hydration.  ClearSite is able to absorb 2-1/2 times its weight in wound
exudate and maintains its  structural  integrity and wound healing  capabilities
for up to seven days. It provides a  biocompatible,  moist  healing  environment
that conforms to the skin,  cushions and produces a cooling  effect at the wound
site.

         NDM  first  introduced  ClearSite  to the  market  in  early  1992  and
currently  produces ClearSite wound dressings in a number of sizes and forms for
use in a variety of  applications,  depending on the type of wound, the location
of the wound and the patient.  ClearSite is available in several different sizes
of patches, with and without a foam adhesive border, in bandage rolls and island
dressings. In August 1994, NDM introduced its island dressing form of ClearSite.
The island dressing has a clear, breathable, pliable, adhesive polyurethane film
border, which is more conformable to certain parts of the human body.

         The  Company  recently   released  a  new  wound  care  product  called
HydrogauzeTM, which NDM developed as a bridge between traditional gauze bandages
and advanced occlusive wound dressings. Hydrogauze is a gauze-like material that
has been impregnated  with dehydrated  ClearSite that hydrates upon contact with
wound exudate.  Hydrogauze combines the look and feel of gauze bandages with the
wound healing  advantages of Clearsite  hydrogel.  NDM plans to develop  several
different formulations of Hydrogauze for use in a variety of applications,  such
as chronic and acute wounds, burns and donor sites for skin grafts.

         NDM's  Act One  Foot  Pump is  designed  to treat  various  circulatory
conditions,  such as decubitus ulcers,  venous stasis ulcers and related chronic
wounds.  The pump is also  used as  prophylaxis  against  deep  vein  thrombosis
("DVT").  DVT  fatally  affects  approximately  250,000  people per year with an
additional 1,700,000 affected by venous disorders. DVT is a blood clot formed in
the leg  which  can break  loose,  travel  to the  lungs  and cause a  pulmonary
embolism  (the  closure  of a blood  vessel in a lung  caused  by a blood  clot)
resulting in death.  Venous stasis ulcers affect  approximately  850,000 people.
The Company believes that the U.S. market for compression products,  such as the
Act One Foot Pump,  used as a prophylaxis to treat DVT is at least $100 million.
Approximately  10  million   Americans  suffer  from  a  combination  of  severe
ulcerations of the lower  extremities,  ischemic rest pain (pain  resulting from
poor circulation) or painful varicose veins. NDM has received clearance from the
FDA to market the foot pump as a prophylaxis against DVT and for increased blood
flow and circulation.

         The Act One Foot Pump  consists of a pneumatic  pump and a foot slipper
with dual bladders  surrounding the foot that mechanically force venous blood to
return to the heart. The pressure of the impulse  delivered to the foot, as well
as the length of time between  pumping can be  programmed  into the Act One Foot
Pump.  NDM believes that its  proprietary  dual bladder  system has  significant
advantages  over single  bladder  systems used by its  competitors,  including a
better fit and improved  blood flow  velocity.  The Act One foot slipper is also
very easy to use for  clinical  personnel  or for  in-home  use.  By pumping the
circumference  of the foot,  the Act One  restores a more normal blood supply to
the leg.  Once this process is achieved,  other  treatments  can also be used to
enhance  healing  the  patient's  wounds.  The  benefits  to  patients  of  foot
compression  pump  treatment  include  reduced  incidence  of DVT,  reduction of
post-operative pain and swelling, and healing of chronic ulcer wounds.

         Patient care products generated  revenues of approximately  $1,380,000,
$3,312,000, and $3,850,000 in the fiscal years ended December 31, 1992, 1993 and
1994, respectively.

         Critical Care Division

         NDM's  critical care division  consists of  electrodes,  cable and lead
wires and electrosurgical products.

         Electrocardiograph    ("ECG")   monitoring   electrodes   account   for
approximately  two-thirds of NDM's revenues.  Electrodes are designed to provide
an  interface   with  the  patient   which  is  capable  of  sensing  low  level
electrocardiographic  signals from the heart and  converting  them to electronic
signals that can be interpreted by monitoring and recording equipment. Long-term
electrodes are used for  continuous  ECG monitoring for use in operating  rooms,
emergency rooms, recovery rooms, and intensive care units. Diagnostic electrodes
are used for specific diagnostic tests of the heart, including ECG tests, stress
tests, Holter monitoring and  echocardiography  tests.  Specialty electrodes are
used in hospital  departments  with specific  needs,  including  neonatal units,
cardiac catheterization labs, and magnetic resonance imaging units.

         The worldwide  market for electrodes was estimated to be  approximately
$200 million in 1992. NDM believes that the electrode  market is a mature market
with only minimal  growth  potential.  Purchase  decisions are generally made on
acceptable level of product performance and cost-effectiveness to the buyer.

         NDM  believes  that it is one of the most  efficient  manufacturers  of
electrodes in the United States.  NDM  attributes  its  efficiency  primarily to
three factors:  (a) NDM coats its electrodes with its own proprietary  adhesive;
(b) NDM  manufactures  its own  hydrogel;  and (c)  NDM  uses  highly  automated
production  equipment  which  significantly  reduces its cost of production.  In
addition,  the  Company  believes  that its  electrodes  are as  advanced as any
electrode  currently on the market.  NDM has used its  ClearSite  technology  to
enhance  its  electrodes,  and most NDM  electrodes  have  ClearSite  gel bonded
directly  onto the active  portion of the  electrode  patch.  In addition to the
characteristics   discussed  above,  ClearSite  is  an  excellent  conductor  of
electricity.  By bonding  ClearSite onto the electrode patch, NDM has provided a
dry gel conductor for adult monitoring electrodes. As a result, NDM's electrodes
are comfortable to the patient, do not require the typical clean-up of a wet gel
and are convenient for the medical  technician.  The Company recently introduced
its Silvon(R) foam electrode and Plia-Cell(R) cloth electrode, both of which are
X-Ray  translucent  and are  designed  to  provide a standard  adult  monitoring
electrode for use in a variety of applications.

         NDM's line of disposable,  pregelled  electrodes include cloth and foam
monitoring   electrodes,   stress  and   diagnostic   electrodes  and  specialty
electrodes, such as, peripheral nerve stimulation electrodes,  X-Ray translucent
electrodes and pediatric and neonatal electrodes. NDM's research and development
activities and the development of ClearSite  hydrogel has led to advancements in
NDM's  electrodes.   NDM's  Silvon(R)  foam  electrode  and  Plia-Cell(R)  cloth
electrode  contain a carbon  stud,  rather than a metal stud,  which makes these
electrodes X-Ray translucent.  The Silvon diaphoretic and Plia-Cell  diaphoretic
electrodes  have a specially  formulated  adhesive to  withstand  the effects of
heavy perspiration. In order to contain costs, hospitals are reducing the number
of vendors  from whom they  purchase  supplies  and the number of products  they
purchase.  NDM  developed  the  Silvon  and  Plia-Cell  electrodes  to provide a
standard adult monitoring  electrode that could be used in a variety of hospital
applications.  The Company has also recently  introduced  its Profile  electrode
which has the same design as the Silvon and  Plia-Cell  electrodes,  except that
the Profile electrode has a metal stud.

         NDM also manufactures and markets ECG monitoring  cables,  reusable and
disposable  lead wire  products and  accessories.  ECG cables and lead wires are
reusable  products  designed to transmit ECG signals  from the heart  (converted
into  electrical  signals by an electrode)  to an ECG monitor or recorder.  Lead
wires  connected  directly to the electrodes are plugged into the patient end of
the  cable.  Cables are  designed  to accept  from  three to fifteen  lead wires
depending  on the level of  monitoring  required.  The  machine end of the cable
plugs  directly into the receptacle of the  monitoring  equipment.  NDM produces
radio  translucent lead wires that are non-metallic and do not obstruct the view
under the X-Ray or fluoroscope.

         NDM's  electrosurgical  products consist of  electrosurgical  grounding
pads,  pencils and  generators  and Endoflex  flexible  retractors for minimally
invasive  surgery.  According to industry  estimates,  approximately  22 million
surgical procedures were performed in 1993,  approximately 65% of which involved
electrosurgery.  It is  estimated  that  by  1995,  20% - 25%  of  all  surgical
procedures will be performed laparoscopically (a minimally invasive technique in
which small incisions are made in the body and surgical procedures are performed
through  small tubes  inserted in the  incisions).  NDM expects the  increase in
minimally  invasive  procedures  to  increase  demand  for its  grounding  pads,
generator and Endoflex  products,  but to reduce demand for its  electrosurgical
pencils.   According  to  industry  estimates,  the  worldwide  market  for  the
electrosurgical  products offered by NDM was approximately  $160 million in 1992
(including   approximately  $70  million  in  grounding  pads,  $40  million  in
generators, and $50 million in electrosurgical pencils).

         NDM manufactures and sells two disposable  grounding pad products which
return the electric  current from the patient to the  generator:  the Neoflex(R)
conductive grounding pad and the DiaTemp II(R)  capacitively-coupled  dispersive
grounding pad. The Neoflex  incorporates  NDM's  ClearSite  hydrogel  technology
which enhances  conductivity,  optimizes patient skin contact and removes easily
without leaving residue. Both models can be used with most available generators.
The  DiaTemp  II  pad  has  an  adhesive  dielectric  membrane  which  disperses
electrical  current evenly over the entire membrane surface for uniform heating,
reducing the risk of patient skin burns. NDM believes that the DiaTemp II is the
most  cost-effective and safest grounding pad in the industry,  and NDM has been
issued patents which cover various aspects of the dispersive technology.

         NDM's PowerPoint electrosurgical pencils are hand-held surgical devices
used by the surgeon to apply the RF current to the surgical  site. The pencil is
available in three  configurations  to accommodate  surgeon  preference  (rocker
switch, push-button switch and foot switch).

         NDM markets and sells an electrosurgical  generator, the PowerPoint(TM)
1000,  which is  manufactured  on an OEM  basis  for NDM by a third  party.  The
PowerPoint  1000,  which  is  designed  for  general  operating  room  use,  has
adjustable  power  settings  for  cutting  only,  a  combination  of cutting and
coagulating, and pinpoint and spray fulguration. The PowerPoint 1000 operates in
the  monopolar  and  bipolar  modes and can be used  with  most  electrosurgical
accessories and supplies, whether manufactured by NDM or other companies.

         NDM also markets Endoflex flexible  retractors for organ retraction and
manipulation in minimally  invasive  surgery.  Endoflex is a surgical  retractor
that consists of a straight shaft with an activation  handle at the proximal end
and a flexible, segmented portion at the distal end. The segmented portion takes
a pre-formed  shape when  activated.  This design  allows the  instrument  to be
inserted into a cannula during a laparoscopic procedure, after which the surgeon
forms it into one of a series of hooks, angled hooks,  triangular retractors and
mildly curved  instruments.  Each one of the instruments  enables the surgeon to
hold  tissues  and  retract  or  manipulate  organs  in much  the  same way as a
surgeon's hands and fingers would in an open procedure.

         Critical care products generated revenues of approximately $31,386,000,
$29,969,000  and  $28,430,000 in the fiscal years ended December 31, 1992,  1993
and 1994, respectively.

Marketing And Distribution

         The principal United States market for NDM's products are hospitals and
alternate care sites, such as clinics,  physician  offices,  ambulatory  surgery
centers  and nursing  homes.  NDM's sales  activities  are  directed by its Vice
President  of Sales who manages  approximately  30 direct sales  personnel.  The
Company  also  maintains  customer  service and  telemarketing  functions at its
office in Dayton,  Ohio to support  the sales  staff.  NDM's Vice  President  of
Marketing  manages the  marketing  department,  which also  includes a number of
product  managers.   The  marketing  department  is  responsible  for  marketing
activities  for both the patient care and  critical  care  divisions,  including
clinical studies, advertising promotion and other related marketing functions.

         The field  sales  force is  trained in the  technical  aspects of NDM's
products  and their uses.  They  provide  hospital  personnel  with  information
relating to the  technical  features and benefits of NDM's  products.  The field
sales force also coordinates sales efforts within geographic territories,  works
with distributors and maintains  relationships  with the hospitals and alternate
care sites.  While  NDM's  sales  efforts are  directed  towards  hospitals  and
alternate  care sites,  NDM's  products  are  generally  purchased  by hospitals
through  distributors.  NDM normally  sells its products in the United States to
distributors  which then resell the products to  hospitals  and  alternate  care
sites.  The Company  generally sells capital  equipment,  such as generators and
foot pumps, directly to hospitals and alternate care sites.

         NDM's marketing  programs  include  development of product  literature,
attendance at major national and international  medical conventions,  sponsoring
clinical studies, direct mail advertising,  telemarketing, promoting publication
of abstracts  and journal  articles  demonstrating  the  effectiveness  of NDM's
products and other  various  promotional  and product  support  activities.  For
example,  several studies have been conducted demonstrating the effectiveness of
ClearSite  hydrogel  wound  dressing  products.  NDM is committed to  sponsoring
studies for its hydrogel wound dressings and its Act One Foot Pump.

         In recent years,  the  distribution of medical products to hospitals in
the United States has been characterized by significant consolidation, primarily
to reduce  inventory and purchasing  costs.  To increase  efficiency,  hospitals
generally purchase most of their medical products directly from a limited number
of large  distributors.  The  largest  distributors  of medical  products in the
United  States are Baxter  Healthcare,  Owens & Minor and  General  Medical.  In
addition,  hospitals have been forming large national and regional buying groups
in order to purchase  products at more  favorable  prices.  Alternate care sites
generally purchase medical products through these large distributors, as well as
a larger number of smaller regional distributors.

         In addition to the distribution agreement NDM has with Baxter, which is
discussed below, NDM has entered into non-exclusive  distribution agreements for
hospital sales with Owens & Minor, General Medical, Colonial, Burrows and Medix.
NDM  has  also  entered  into  oral   agreements   with  over  50   independent,
non-exclusive  distributors who sell NDM's products  primarily to alternate care
sites.  Some of these  alternate  care site  distributors  may  eventually  sell
products  to  some  hospitals,  as  well.  NDM has  also  entered  into  written
agreements with a number of national hospital buying groups.

         NDM recently  exercised its right to extend the distribution  agreement
with Baxter through December 31, 1995;  however,  under the current terms of the
extension,  Baxter's margins will increase,  resulting in an expected additional
cost to NDM of  approximately  $700,000  in 1995.  NDM and Baxter are  currently
negotiating a new  distribution  agreement  which,  if  consummated  on proposed
terms,  would produce generally  comparable  margins for NDM in 1995 as in 1994.
Under the current  agreement,  Baxter has the exclusive  right to distribute the
Company's  critical care products to approximately  one thousand U.S.  hospitals
that were  customers  of Baxter on  January  1, 1992,  and the  Company  has the
exclusive  right to  provide  those  products  to  Baxter.  Baxter  also has the
non-exclusive  right to distribute the Company's critical care products to other
U.S.  hospitals and the non-exclusive  right to distribute the Company's patient
care  products  to U.S.  hospitals.  Virtually  all  sales of  NDM's  disposable
products to U.S. hospitals are made through major hospital distributors.  Baxter
is  by  far  the  largest   distributor  of  NDM's   products,   accounting  for
approximately  95% of NDM's  sales to U.S.  hospitals.  NDM has  taken  steps to
reduce  its  dependence  on  Baxter  by  selling  its  products   through  other
distributors  and plans to  continue to broaden its  distribution  network.  NDM
estimates that Baxter  currently  controls  approximately  30% of the market for
distribution  of medical  products to United States  hospitals.  There can be no
assurance  that NDM will be able to  negotiate  a new  agreement  with Baxter on
terms  favorable to NDM or that Baxter will continue to distribute the Company's
products. If NDM is unable to negotiate an agreement with Baxter satisfactory to
NDM, the Company would be materially adversely affected.

         The Company's European sales consist primarily of patient care products
which are distributed through independent distributors. NDM's distributor in the
United Kingdom  assists NDM in managing NDM's network of European  distributors.
NDM currently has written  agreements with international  distributors  covering
Japan, Germany, Austria, Belgium, Australia, Luxembourg, the United Kingdom, The
Netherlands,  Denmark,  and New Zealand and oral agreements  with  international
distributors  covering  various  other  countries.  NDM  also  manufactures  its
hydrogel  wound dressing  products on an OEM basis for some of its  distributors
and competitors.

Competition

         The medical  device  industry is  intensely  competitive  in almost all
segments and tends to be dominated in large, more mature markets by a relatively
small group of large,  well-financed  companies.  Most of NDM's competitors have
significantly  greater  financial,  marketing and other  resources than NDM. NDM
also competes with smaller,  more entrepreneurial  companies,  some of which are
better  financed  than NDM and already  have  established  positions  in certain
markets.  The Company believes that it competes favorably in its current markets
based on product quality, technology and pricing.  Furthermore,  the health care
industry is currently  undergoing  significant  consolidation in part to control
health care costs. In particular,  Conmed Corp.  recently  announced that it has
agreed to acquire Birtcher Medical Systems,  Inc., both of which are competitors
of the Company.

         Patient Care Division

         NDM  estimates  that  hydrocolloid   products   currently  account  for
approximately 95% of the absorbent  occlusive dressing market, of which hydrogel
wound  dressing  products are a part.  The dominant  competitor in the occlusive
dressing market is Convatec Inc., a division of  Bristol-Meyers  Squibb Company,
which  produces the  hydrocolloid  product  Duoderm.  NDM estimates that Duoderm
accounts for up to 75% of the hydrocolloid  segment of this market and generates
annual  revenues  greater than $100 million.  NDM believes that the remainder of
the hydrocolloid market is shared among a number of other manufacturers, none of
which has a significant market share. NDM's primary  competition for moist wound
dressing products,  which are gel-based  technologies,  include Vigilon Products
manufactured  by Bard Home  Health  Inc.,  NuGel(R),  manufactured  by Johnson &
Johnson  Medical  Products,  Inc., and  Elastogel(R)  manufactured  by Southwest
Technology.

         NDM estimates that The Kendall Company  currently has approximately 80%
of the U.S. market for compression  pumps. In addition,  Kendall  distributes in
the U.S. the foot pump manufactured by NovaMedix Ltd., which is the subject of a
patent infringement  involving the Company. See Item 3 - Legal Proceedings.  The
Company believes that its foot pump has superior  technology and will be able to
compete effectively with the NovaMedix foot pump.

         Critical Care Division

         The principal  competitors in the electrode  market are 3M Corporation,
Conmed Corporation and Graphic Controls Inc., with 3M controlling  approximately
30% of the market.  NDM believes that it currently has the third largest  market
share,  with  approximately  14%  of  the  market.   Electrodes  have  become  a
"competitive"  product,  and the Company believes that cost will be an important
competitive factor in this market as a result of continuing cost control efforts
by  hospitals.  NDM  has  taken  measures  that it  believes  will  improve  its
competitive  position  by  incorporating  hydrogel  technology  into  all of its
electrodes, lowering production costs, providing a standardized adult monitoring
electrode for use in a wide variety of applications and consolidating  redundant
product  lines.  The  installation  of new  automated  production  equipment  in
December 1993 has reduced NDM's manufacturing cost  significantly.  NDM believes
that it is one of the most efficient manufacturers of electrodes.

         NDM's  principal  competitor  for cable and wire  products  is Tronomed
Inc., a subsidiary of Graphic  Controls.  NDM believes that competitive  pricing
and new  product  features  are  critical  to the  success of its cable and wire
product products, as well as enhancing sales of its ECG electrodes.

         NDM's  principal   competitors  in  the   electrosurgical   market  are
ValleyLab,  a division of Pfizer, Inc., Birtcher Medical Systems,  Inc., Zimmer,
3M Corporation,  and Conmed  Corporation.  NDM estimates that ValleyLab controls
approximately 55%-65% of the segments of the electrosurgical market in which NDM
competes. NDM does not have a significant market share in any of these segments.

Manufacturing And Supplies

         NDM  manufactures  or assembles its products at its facility in Dayton,
Ohio. NDM's vertically integrated manufacturing process allows it to obtain cost
efficiencies by purchasing raw materials for its hydrogel and electrode products
in bulk and converting  those  materials into the parts and pieces used in final
assembly.  NDM uses various manual,  semi-automated and automated  equipment for
fabrication  and assembly of its products and is continuing to further  automate
its  facilities  to remain  competitive.  In December  1993,  NDM  installed new
automated  equipment  for the  production  of its newest  electrodes,  which has
resulted in significant  savings in production  costs. As a result,  the Company
believes that it is one of the most efficient manufacturers of electrodes in the
United States.

         NDM purchases  virtually all of the raw materials for its products from
domestic suppliers.  Although the Company has multiple sources or has identified
second  sources  for most of these raw  materials,  it has only one  source  for
certain  raw  materials  used in the  production  of some of its  products.  The
Company is seeking  second sources for all of the  single-sourced  raw materials
used in its products,  although  there can be no assurance that NDM will be able
to obtain suitable second sources. To the Company's  knowledge,  other electrode
manufacturers,  as well as NDM,  are  dependent  on the same single  sources for
certain components used in electrodes.  NDM is also dependent on these suppliers
for  certain  components  used  in its  grounding  pads.  In  addition,  certain
suppliers  have  recently  indicated a reluctance to supply raw materials to the
medical industry due to the risk of liability to these suppliers. The failure of
any one of the  Company's  sole sources of critical raw materials to supply such
materials would have a material adverse effect on the Company.

Research And Development

         NDM believes that its research and  development  capability is an asset
which  will  be  critical  to its  future  growth.  NDM  conducts  research  and
development  primarily  at its  facility in Dayton,  Ohio,  although the various
clinical  studies which it sponsors are generally  conducted in laboratories and
clinics at  universities  and  hospitals  around the world.  NDM's  research and
development  is focused on improving  and expanding  existing  product lines and
developing  new  products.  NDM has developed  most of its products  internally,
including the ClearSite hydrogel  technology,  which NDM initially  developed to
improve  its  electrodes.   NDM  has  also  invested  significant  research  and
development  resources  in its  adhesive  technology  which is used in ClearSite
hydrogel,  electrodes and electrosurgical grounding pads. NDM also developed its
electrodes internally.

         NDM's  research  and  development   expenditures   were   approximately
$885,000, $1,036,000 and $1,145,000 in the fiscal years ended December 31, 1992,
1993 and 1994, respectively.

Patents and Proprietary Protection

         NDM seeks to  protect  its  intellectual  property  through  the use of
patents, trade secrets,  trademarks,  and copyrights. NDM believes that reliance
upon trade secrets and  unpatented  proprietary  know-how,  the  improvement  of
existing  products,  and  the  development  of new  products  are  generally  as
important as patent  protection in  establishing  and  maintaining a competitive
advantage.  Nevertheless,  NDM has obtained and will  continue to seek  patents,
when available, in connection with its product development program. Although NDM
has been granted United States patents on certain features of its products,  and
has applied for others,  there can be no  assurance  that any patent held by the
Company  will be valid or  otherwise  of value to the Company or that any patent
application  currently  pending will be granted.  In  addition,  a number of the
Company's  patents  covering  its  electrodes  will expire over the next several
years. Even with significant patent protection, the Company may be vulnerable to
competitors who attempt to copy its products. While the Company has successfully
defended and enforced  its patents in the past,  there can be no assurance  that
the  Company  will be able  to do so in the  future.  The  Company  also  relies
extensively on trade secrets and unpatented  proprietary know-how,  particularly
in the  formulation and production of its hydrogel  technology.  There can be no
assurance  that the Company will be successful  in protecting  its trade secrets
and  unpatented  proprietary  know-how.  While the  Company  believes it has all
rights   necessary  to  manufacture  and  sell  its  current   products  without
infringement  of patents held by others,  the Company has not conducted a formal
infringement  search and there can be no assurance that such conflicting  rights
do not exist. In particular,  NDM is currently  defending a patent  infringement
action brought by Novamedix Limited relating to NDM's Act One Foot Pump. NDM has
obtained  an  opinion  from its  patent  counsel  that  NDM's foot pump does not
infringe the Novamedix patent, and NDM is vigorously defending its position.  If
NDM is  unsuccessful  in defending its position,  NDM's strategy with respect to
its Act One Foot Pump would be adversely affected.

         NDM has  obtained  a number of  registered  trademarks  including  NDM,
ClearSite,  Silvon, Plia-Cell,  ResTest, Accutac, NDM High Demand,  TenderTrace,
Nu-Connect,  V-Trace,  Neoflex, DiaTemp and PowerPoint.  NDM has filed trademark
applications  on  Hydrogauze,  PinSite and Profile.  In addition,  NDM has filed
trademark  applications  on some of its other  products  and in certain  foreign
countries.

Regulation

         The medical  devices  manufactured  and  marketed by NDM are subject to
regulation  by the United  States Food and Drug  Administration  ("FDA") and, in
some instances, by state and foreign authorities. Pursuant to the Medical Device
Amendments of 1976 ("1976  Amendments")  to the Federal Food,  Drug and Cosmetic
Act, and regulations promulgated thereunder,  medical devices intended for human
use are classified  into three  categories  (Classes I, II, and III),  depending
upon the degree of  regulatory  control to which  they would be  subject.  NDM's
current products have been classified as Class I or Class II devices.

         If a new device,  irrespective of whether it is a Class I or II device,
is  substantially  equivalent to an existing  device that has been  continuously
marketed  since the  effective  date of the 1986  Amendments  (May 28,  1976) (a
"Substantially  Equivalent Device"), FDA requirements may be satisfied through a
Premarket  Notification  Submission  (a "510(k)  Submission"),  under  which the
applicant  provides  product  information  supporting  its claim of  substantial
equivalence.  In a  510(k)  Submission,  the FDA  may  also  require  that it be
provided with clinical test results demonstrating the safety and efficacy of the
device.  If a  medical  device  does  not  qualify  for  the  510(k)  Submission
procedure,  the manufacturer must file a pre-market approval application,  which
requires more extensive testing than the 510(k) Submission  process and involves
a  significantly   longer  FDA  review  process.   NDM  regularly  files  510(k)
Submissions for new products and improvements to existing products.

         Although the 510(k)  Submission  process was originally  designed to be
relatively fast, recent  legislation,  regulations,  and policy decisions by the
FDA have made the 510(k)  Submission  process  substantially  more difficult and
time-consuming than in the past. There can be no assurance that NDM or any other
manufacturer of medical equipment will be able to obtain clearances or approvals
for new products or product  improvements in the future on a timely basis, or at
all. Any  significant  delay in obtaining the necessary  approvals  could have a
material adverse effect on NDM.

         As a manufacturer  of medical  devices,  NDM is also subject to certain
other FDA regulations and its manufacturing processes and facilities are subject
to continuing  review by the FDA to ensure  compliance  with Good  Manufacturing
Practices  regulations.  NDM believes that its manufacturing and quality control
procedures  substantially  conform to the requirements of FDA  regulations.  The
Company  underwent  a GMP  inspection  in  February  1994 and was found to be in
compliance with GMP regulations.

         NDM's products are also subject to regulation in foreign countries.

Employees

         As of December 31, 1994, NDM had approximately 204 full-time employees,
including 10 in research and development, 125 in manufacturing,  41 in sales and
marketing, and 28 in general and administrative functions.

Item 2.   PROPERTIES.

         NDM's  administrative,  manufacturing,  and  research  and  development
facilities  are  located  at 3040 East  River  Road,  Dayton,  Ohio  45439.  The
facilities consist of approximately 100,000 square feet and are owned by NDM.

Item 3.   LEGAL PROCEEDINGS.

         On April 8, 1994, Aspen  Laboratories,  Inc.  ("Aspen") filed an action
against NDM in the United  States  District  Court for the Southern  District of
Ohio (Western Division-Dayton) Civil Action No. C-3-94-152.  Among other things,
the complaint  alleges that (i) Aspen is the sole owner of all right,  title and
interest in and to a certain patent and invention  pursuant to a patent duly and
legally  issued  by the  U.S.  Patent  and  Trademark  Office  entitled  "return
electrode  contact  monitor" (the  "Patent"),  (ii) NDM is offering for sale and
selling  under the NDM name certain  return  electrode  contact  monitors  which
infringe claims of the Patent,  and (iii) NDM's actions have encouraged,  aided,
abetted and actively  induced  infringement by others and/or have contributed to
infringement by others of the Patent.  Aspen's claims for relief include,  among
other  things,  that NDM be  enjoined  against  infringing,  inducing  others to
infringe, or contributing to the infringement by others upon the Patent and that
an accounting of all NDM's sales and profits  derived from the  infringement  be
undertaken, and that Aspen be compensated in damage for such infringement.  This
action has been stayed pending  resolution of other litigation,  in which NDM is
not a party,  involving similar issues.  Aspen's parent  corporation  ConMed has
acquired Birtcher Medical Systems,  which manufactures the product for NDM on an
OEM basis. Accordingly, the Company believed this lawsuit will be dismissed.

         On June 10, 1994, NovaMedix, Limited filed an action against NDM, Vesta
Healthcare,  Inc. and the Hall Company,  in United States District Court for the
Southern  District  of Ohio,  Western  Division  at  Dayton,  Civil  Action  No.
C-3-94-251.  NovaMedix  alleges  that  defendants  are  infringing  upon several
patents by making,  using and selling medical  devices,  including NDM's Act One
Foot Pump and associated  inflatable  bladders and slippers embodying the patent
inventions without license from NovaMedix. NovaMedix seeks an injunction against
defendants  from further  infringement  of the patents,  damages for the alleged
infringement in an amount not less than a reasonable royalty with interest,  and
triple  damages  for  the  alleged   willful  and   deliberate   nature  of  the
infringement,  together with an award to NovaMedix of its  reasonable  attorneys
fees.  NDM has obtained an opinion from its patent counsel that the Act One Foot
Pump does not infringe the NovaMedix patent, and NDM is vigorously defending its
position.

         In October  1994,  NovaMedix  filed a similar  action NDM in the United
Kingdom relating to a U.K. patent that would affect marketing the product in the
U.K.  The Company  does not believe  that it  infringes  the U.K.  patent and is
vigorously defending its position. NDM has answered these complaints and expects
a trial in the United Kingdom in June 1995.

Item 4.   SUBMISSION OF MATTERS TO A VOTE OF SECURITY HOLDERS.

         No matter was submitted to a vote of security holders during the fourth
quarter of the fiscal year covered by this Annual Report.

                                    PART II

Item 5.  MARKET FOR THE REGISTRANT'S COMMON STOCK AND RELATED
         SECURITY  HOLDER MATTERS.

Market Information

         As of March 31, 1995,  4,311,977 shares of Common Stock were issued and
outstanding.  There is currently no established trading market.  Pursuant to the
Plan of  Reorganization,  the  Company  intends  to  submit an  application  for
inclusion of the Common Stock on the National  Association of Securities Dealers
Automated  Quotation  ("NASDAQ")  System. See "BUSINESS-  Background."  However,
there can be no assurance that such application will be approved, and until such
time the Company expects the Common Stock to be traded on local over-the-counter
markets.

Holders

         Following the  distribution of the Common Stock pursuant to the Plan of
Reorganization,  the Company expects to have approximately 1,000 shareholders of
record.

Dividends

         The Company currently intends to retain any future earnings to fund the
development of its business and therefore  does not  anticipate  paying any cash
dividends  on its  Common  Stock  in the  foreseeable  future.  The  Company  is
prohibited  under its credit facility from paying  dividends on its Common Stock
without the consent of the lender.


Item 6.   SELECTED FINANCIAL DATA.

         The selected consolidated financial data on the following page for, and
as of the end of, each of the years in the four year period  ended  December 31,
1993 as well as the selected  consolidated  financial data for the periods ended
October 14, 1994 and December 31, 1994, have been derived from the  consolidated
financial  statements of MEI Diversified  and New Dimensions In Medicine,  Inc.,
which have been audited by Arthur Andersen LLP,  independent public accountants.
The  auditor's  report on MEI  Diversified  is qualified  due to an inability to
obtain written  representations  regarding  certain matters from MEI Diversified
Management. The auditor's reports for both MEI Diversified and New Dimensions In
Medicine,  Inc.  contain an  explanatory  paragraph  related to their ability to
continue as a going  concern.  The selected  consolidated  financial  data as of
October 15, 1994 and December  31, 1994 have been derived from the  consolidated
balance sheets of New Dimensions In Medicine,  Inc.,  which have been audited by
Arthur Andersen LLP,  independent public accountants.  This report also contains
an explanatory  paragraph  related to the ability of New Dimensions In Medicine,
Inc. to continue as a going  concern.  The  consolidated  balance  sheets of New
Dimensions  In  Medicine,  Inc. as of October 15, 1994 and December 31, 1994 and
the consolidated financial statements for the 10-week period ending December 31,
1994, and the  consolidated  financial  statements of MEI Diversified Inc. as of
October 14, 1994 and  December  31, 1993 and for the 42 weeks ended  October 14,
1994 and for each of the years in the two year period  ended  December 31, 1993,
and the reports  thereon,  are  included  elsewhere in this Annual  Report.  The
selected consolidated financial data information is qualified in its entirety by
reference  to such  consolidated  financial  statements  and  should  be read in
conjunction  with  the  consolidated   financial   statements   included  in  or
incorporated by reference into this Annual Report.

         Effective as of October 15, 1994,  the day after the effective  date of
the Plan of  Reorganization,  the Company  adopted "fresh start"  accounting for
financial  reporting  purposes in  accordance  with the  American  Institute  of
Certified Public Accountants Statement of Position 90-7, "Financial Reporting by
Entities  in  Reorganization  Under  the  Bankruptcy  Code."  The  effect of the
adoption  of  Statement  of  Position   90-7  is  reflected  in  the   Company's
consolidated  balance sheet as of October 15, 1994.  Accordingly,  the Company's
consolidated  balance sheet at and after  October 15, 1994 and its  consolidated
statements of operations, cash flows and changes in stockholders' equity for the
periods  thereafter  are not, and will not be,  comparable  to the  consolidated
financial  statements of MEI  Diversified  Inc. for the periods prior to October
15, 1994,  that are set forth below and certain of which are included  elsewhere
in this Annual  Report.  The  consolidated  balance  sheets of New Dimensions In
Medicine,  Inc., and the  consolidated  financial  statements of MEI Diversified
Inc. and the notes thereto should be referred to for  additional  information on
certain of the periods presented on the following page.

Statements of Operations Data:
(All Data Except Per Share Data in Thousands)
Post Pre Reorganization Reorganization -------------- --------------------------------------------------- 10 Weeks 42 Weeks Ended Ended Year Ended December 31, December 31, October 14, --------------------------------------------------- 1994 1994 1993 1992 1991 1990 --------- --------- --------- --------- --------- --------- Revenues ........................................ $ 7,398 $ 24,882 $ 33,281 $ 32,766 $ 32,512 $ 15,596 Operating income (loss) ......................... 586 (4,516) (2,372) (853) (1,797) (2,887) Income (loss) from continuing operations ........ 252 (15,275) (11,281) (7,002) (8,039) (5,847) Income (loss) from discontinued operations .................................... -- 352 (4,021) (103,218)(1) (4,611) (6,097) Net income (loss) ............................... 252 (14,923) (15,302) (110,220) (12,650) (11,944) Per common share: Income (loss) from -- continuing operations ....................... 06 (.82) (.60) (.37) (.43) (.30) discontinued operations ..................... -- .02 (.22) (5.53) (.24) (.32) Net income (loss) ............................. 06 (.80) (.82) (5.90) (.67) (.62) Weighted average number of common shares outstanding ...................... 4,312(2) 18,686 18,686 18,685 18,746 19,206
- ---------------- (1) Primarily represents losses incurred in connection with the discontinuance of the professional beauty salon operations. (2) As of December 31, 1994, the Company was still in the process of distributing the shares of common stock to shareholders. For financial reporting purposes, net income per share has been computed based upon the weighted average number of shares outstanding during the period on a pro forma basis. Balance Sheet Data: (In Thousands)
Post Pre Reorganization Reorganization -------------- --------------------------------------------------- Fresh-Start Historical as of As Of December 31, December 31, October 15, --------------------------------------------------- 1994 1994 1993 1992 1991 1990 --------- --------- --------- --------- --------- --------- Working capital (deficit) .......................... $ 3,485 $ 3,169 $ 8,298 $(103,264) $ 25,640 $ 41,739 Total assets ....................................... 34,425 35,677 85,132 90,605 190,650 274,586 Pre-petition liabilities subject to compromise ............................ -- -- 116,327 -- -- -- Long-term debt, less current maturities ............ 5,204 5,605 9 -- 101,362 115,875 Stockholders' equity ............................... 18,752 18,500 (50,513) (35,211) 74,963 86,429
PRO FORMA FINANCIAL INFORMATION The following pro forma consolidated balance sheet gives effect to the Plan of Reorganization as of October 15, 1994, the day after the effective date of the Plan of Reorganization. The pro forma consolidated balance sheet has been prepared on the "fresh-start" basis of accounting prescribed by American Institute of Certified Public Accountants Statement of Position 90-7, on Financial Reporting by Entities in Reorganization Under the Bankruptcy Code. The unaudited pro forma statements of operations for the 42 weeks ended October 14, 1994, and the year ended December 31, 1993 give effect to the Plan of Reorganization as if it had occurred, and such transactions had been consummated as of January 1, 1993. The following pro forma financial information does not purport to represent what the Company's actual results of operations or financial position would have been had the effective date in fact occurred, and had such transactions in fact been consummated, at the beginning of each of these periods. The pro forma financial information does not give effect to any transactions other than those included in the Plan of Reorganization and those discussed in the accompanying Notes to Financial Information, or to the Company's results of operations since October 15, 1994. The following financial information is based upon the historical financial statements of MEI Diversified Inc. as of and for the 42 weeks ended October 14, 1994 and for the year ended December 31, 1993 included elsewhere in this Annual Report, and should be read in conjunction with such historical financial statements, the related notes, and the other information contained in this Annual Report. PRO FORMA CONSOLIDATED BALANCE SHEET (In Thousands)
MEI Consummation Diversified Inc. of Plan of Fresh New Dimensions Assets Historical Reorganization Start In Medicine, Inc. ---------------- -------------- --------- ----------------- Current assets: Cash and cash equivalents .................................. $ 2,647 $ (1,847)(1) $ 0 $ 800 Marketable securities ...................................... 8,500 (8,500)(1) 0 0 Receivables, net ........................................... 4,743 (334)(1) 0 4,409 Receivable from Diversified Liquidating Trust .............. 0 1,258 0 1,258 Inventories ................................................ 8,183 (204)(1) 0 7,979 Prepaid expenses and other current assets .................. 375 (80)(1) 0 295 --------- --------- --------- --------- Total current assets ................................... 24,448 (9,707) 0 14,741 Property, plant and equipment, net ............................. 16,853 (5,319)(1) 0 11,534 Nonoperating real estate ....................................... 4,462 (4,462)(1) 0 0 Goodwill, net of accumulated amortization ...................... 24,990 0 (24,990)(4) 0 Other assets, primarily intangibles ............................ 4,255 (1,774)(1) 6,921 (3) 9,402 --------- --------- --------- --------- Total assets ........................................... $ 75,008 $ (21,262) $ (18,069) $ 35,677 ========= ========= ========= =========
(Continued) PRO FORMA CONSOLIDATED BALANCE SHEET (In Thousands)
MEI Consummation Diversified Inc. of Plan of Fresh New Dimensions Assets Historical Reorganization Start In Medicine, Inc. ---------------- -------------- --------- ----------------- Liabilities and Stockholders' Equity Current liabilities: Revolving line of credit ................................... $ 2,500 $ 0 $ 0 $ 2,500 Current maturities of long-term debt ....................... 826 (20)(1) 0 806 Accounts payable ........................................... 4,982 (876)(1) 0 4,106 Accrued compensation and benefits .......................... 1,862 0 0 1,862 Pre-petition liabilities not subject to compromise ......... 1,993 (1,993)(1) 0 0 Other accrued liabilities .................................. 4,468 (2,170)(1) 0 2,298 --------- --------- --------- --------- Total current liabilities .............................. 16,631 (5,059) 0 11,572 Long-term debt, less current maturities ........................ 5,605 0 0 5,605 Pre-petition liabilities subject to compromise ................. 116,773 (116,773)(1) 0 0 Deferred liabilities ........................................... 285 (285)(1) 0 0 --------- --------- --------- --------- Total liabilities ...................................... 139,294 (122,117) 0 17,177 ========= ========= ========= ========= Stockholders' equity: Common stock, $.05 par value ............................... 962 (962)(5) 0 0 Common stock, $.01 par value ............................... 0 45 (1) 0 45 Common stock warrants ...................................... 2,300 (2,300)(5) 0 0 Unrealized gain on marketable securities ................... 1,150 (1,150)(5) 0 0 Additional paid-in capital ................................. 85,687 18,455 (1) 0 (85,687)(5) 0 18,455 Retained earnings (accumulated deficit) .................... (151,739) 81,097 (1) 0 87,453 (5) 0 1,258 (2) (24,990)(4) 0 6,921 (3) 0 Treasury stock, 562,000 shares, at cost .................... (2,646) 2,646 (5) 0 0 --------- --------- --------- --------- Total stockholders' equity ............................. (64,286) 100,855 (18,069) 18,500 --------- --------- --------- --------- $ 75,008 $ (21,262) $ (18,069) $ 35,677 ========= ========= ========= =========
See Accompanying Notes to Pro Forma Financial Information. NOTES TO PRO FORMA FINANCIAL INFORMATION PRO FORMA CONSOLIDATED BALANCE SHEET (1) To record the following transactions made in connection with the Plan of Reorganization: a) the transfer of assets and liabilities from MEI Diversified Inc. to various Liquidating Trusts established under the Plan of Reorganization; and b) the issuance of New Dimensions In Medicine, Inc. Common Stock including the associated additional paid in capital in connection with the Plan of Reorganization. (2) To record amounts receivable from the Diversified Liquidating Trust pursuant to the Plan of Reorganization. (3) To record adjustments to state the Company's intangible assets at their fair values. (4) To record the write-off of goodwill in accordance with the American Institute of Certified Public Accountants Statement of Position 90-7 on Financial Reporting by Entities in Reorganization Under the Bankruptcy Code. (5) To write off the historical capital structure of the Company. UNAUDITED PRO FORMA CONSOLIDATED STATEMENTS OF OPERATIONS (In Thousands)
For the 42 Weeks Ended October 14, 1994 For the Year Ended December 31, 1993 ---------------------------------------------- ------------------------------------------------------ New New MEI Dimensions In MEI Dimensions In Diversified Inc. Pro Forma Medicine, Inc. Diversified Inc. Pro Forma Medicine, Inc. Historical Adjustments Pro Forma Historical Adjustments Pro Forma ---------- ----------- --------- ---------- ----------- --------- Revenues ................ $24,882 $ 0 $24,882 $33,281 $ 0 $33,281 ------- ------- ------- ------- -------- ------- Costs and expenses: Cost of sales .......... 14,632 (882)(5) 19,277 (1,011)(5) 866 (4) 14,616 885 (4) 19,151 Operating expenses ..... 12,746 (220)(5) 12,648 (253)(5) 216 (4) 221 (4) (86)(6) 138 (7) (415)(6) 204 (7) 12,531 Corporate general and administrative expenses .............. 1,214 (1,214)(1) 0 2,500 (2,500)(1) 0 Amortization of intangible assets ............... 806 (806)(2) 1,228 (1,228)(2) 587 (3) 587 742 (3) 742 ------- ------- ------- ------- -------- ------- Total costs and expenses .............. 29,398 (1,664) 27,734 35,653 (3,092) 32,561 Operating income (loss) ................ (4,516) 1,664 (2,852) (2,372) 3,092 720 Interest expense ...... (371) 1 (1) (370) (1,897) 1,620 (1) (277) Interest income ....... 127 (112)(1) 15 239 (165)(1) 74 Gain (loss) on marketable securities ........... 0 0 0 (700) 700 (1) 0 Other (expense) income, net .......... (6,599) 6,440 (1) (159) (768) 423 (1) (345) ------- ------- ------- ------- -------- ------- Income (loss) from continuing operations before income taxes and reorganization items .. (11,359) 7,993 (3,366) (5,498) 5,670 172 Reorganization items: Professional fees ..... (3,949) 3,949 (1) 0 (5,883) 5,883 (1) 0 Interest earned on accumulated cash ..... 33 (33)(1) 0 100 (100)(1) 0 ------- ------- ------- ------- -------- ------- Income (loss) from continuing operations ............ $(15,275) $11,909 $(3,366) $(11,281) $11,453 $172 ======== ======= ======= ======== ======= ====
(Continued) UNAUDITED PRO FORMA CONSOLIDATED STATEMENTS OF OPERATIONS (Continued) (In Thousands)
For the Quarter Ended December 31, 1993 ---------------------------------------------- New MEI Dimensions In Diversified Inc. Pro Forma Medicine, Inc. Historical Adjustments Pro Forma ---------- ----------- --------- Revenues ................. $8,371 $ 0 $8,371 ------ ------ ------ Costs and expenses: Cost of sales ........... 4,600 (167)(5) 221 (4) 4,654 Operating expenses ...... 3,836 (42)(5) 55 (4) (21)(6) 34 (7) 3,862 (415)(6) Corporate general and administrative expenses ............... 522 (522)(1) 0 Amortization of intangible assets ................. 315 (314)(2) 185 (3) 186 ------ ------ ------ Total costs and expenses ................ 9,273 (570) 8,703 ------ ------ ------ Operating income (loss) .................. (902) 570 (332) Interest expense ........ (76) 1 (1) (75) Interest income ......... (214) 220 (1) 6 Gain (loss) on marketable securities ............. (700) 700 (1) 0 Other (expense) income, net ............ (560) 166 (1) (394) ------ ------ ------ Income (loss) from continuing operations before income taxes and reorganization items .... (2,452) 1,657 (795) Reorganization items: Professional fees ....... (1,127) 1,127 (1) 0 Interest earned on accumulated cash ....... 20 (20)(1) 0 ------ ------ ------ Income (loss) from continuing operations $(3,559) $2,764 $(795) ======= ====== =====
See Accompanying Notes to Unaudited Pro Forma Financial Information. NOTES TO UNAUDITED PRO FORMA FINANCIAL INFORMATION UNAUDITED PRO FORMA CONSOLIDATED STATEMENTS OF OPERATIONS (1) To eliminate the profit and loss effect of former MEI Diversified Inc. subsidiaries as their assets and liabilities have been transferred into the various Liquidating Trusts established under the Plan of Reorganization. (2) To reverse the historical amortization of the excess of cost over fair value of assets acquired and of other intangible assets. Intangible assets include patents and trademarks and are amortized on a straight-line basis over the legal or estimated remaining useful lives of 10 to 15 years. (3) To record amortization expense based on the revised fair value of intangible assets (patents and trademarks). (4) To record depreciation expense based on the revised fair value basis of property, plant and equipment. (5) To reverse the historical depreciation on property, plant and equipment. (6) To reverse the historical amortization expense of start up, marketing and regulatory costs incurred related to new product introductions which were amortized over 36 months. (7) To record start up, marketing and regulatory costs incurred related to new product introductions based on the revised fair value of these costs. Item 7. MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS. Introduction On February 23, 1993, MEI Diversified and certain of its subsidiaries, MEI Salon Corp., Essanelle Salon Co., The Glemby Company, Inc., Maxim's Beauty Salons, Inc., Sophia Beauty Salons (NY), Inc., Glemby International Washington, Inc., Glemby International Missouri, Inc. and Salon Service, Inc. filed voluntary petitions in U. S. Bankruptcy Court (the "Bankruptcy Court") seeking to reorganize under Chapter 11 of the U.S. Bankruptcy Code (the "Bankruptcy Code"). The above filing did not include NDM Acquisition Corp., a former subsidiary of MEI Diversified in which NDM's business had been conducted ("Old NDM") or MEI Diversified's Canadian beauty salon subsidiaries. On September 28, 1994, the Bankruptcy Court extended an order confirming the Plan of Reorganization, and it became effective on October 14, 1994. On October 14, 1994, Old NDM was merged into MEI Diversified, with MEI Diversified being the surviving corporation, pursuant to the Plan of Reorganization. In connection with the merger, MEI Diversified restated its Certificate of Incorporation and changed its name to "New Dimensions In Medicine, Inc." The Company is continuing the business operations of Old NDM. Effective as of October 15, 1994, NDM adopted "fresh start" accounting for financial reporting purposes in accordance with the American Institute of Certified Public Accounts Statement of Position 90-7, "Financial Reporting by Entities in Reorganization Under the Bankruptcy Code." The effect of the adoption of Statement of Position 90-7 is reflected in NDM's Consolidated Balance Sheet as of October 15, 1994. Accordingly, NDM's Consolidated Balance Sheet at and after October 15, 1994 and its Consolidated Statements of Operations, Cash Flows and Changes in Stockholders' Equity for the periods thereafter are not, and will not be, comparable to the Consolidated Financial Statements of MEI Diversified for the periods prior to October 14, 1994. The consolidated financial statements included herein have been prepared on a going concern basis which assumes continuity of operations and realization of assets and liquidation of liabilities in the ordinary course of business. The financial statements reflect the operations of the professional beauty salon subsidiaries as a discontinued operation as a result of the December 1993 sale of the net assets of MEI Salon Corp. and its subsidiaries to a buyer pursuant to Section 363 of the Bankruptcy Code. The financial statements also reflect the operations of the snack food segment as discontinued operations due to the sale of the remaining segment operations in 1992. The following 1994 and 1993 results of continuing operations are on a pro forma basis assuming a going concern and reflect adjustments relating to (a) the Plan of Reorganization, (b) the application of "fresh-start" accounting principles, and (c) the elimination of the profit and loss effects of the former MEI subsidiaries. Results of Continuing Operations for the 10 Week Period Ended December 31, 1994 and for the Quarter Ended December 31, 1993
Pro Forma For the 10 Weeks Ended For the Quarter Ended December 31, 1994 December 31, 1993 ----------------- ----------------- (In Thousands) Revenues $ 7,398 $ 8,371 Cost of Sales 4,286 4,654 Operating Expenses 2,369 3,862 Amortization of Intangible Assets 157 186 Interest Expense 126 75 Interest Income 6 6 Other (Income) Expense, Net (7) 394 Net Income (loss) 252 (795)
Revenue for the Periods Consisted of the Following:
For the 10 weeks Ended For the Quarter Ended December 31, 1994 December 31, 1993 ----------------- ----------------- Critical Care Products 6,248 7,286 Patient Care Products 1,152 1,085 -------- -------- Total Revenue 7,398 8,371 ======== ========
Both critical care and patient care products were impacted by the two week difference in the reporting periods. Patient care products increased despite the two week difference due to the increased wound care revenue during the 10 week period ended December 31, 1994. Cost of sales decreased due to the two week difference in the reporting periods. However, as a percent of revenue the cost of sales for the 10 week period ended December 31, 1994 increased by 2.3% over the fourth quarter of 1993. This is attributed to unabsorbed fixed overhead in manufacturing during the 10 week period ended December 31, 1994 related to an inventory reduction program and the favorable settlement of certain provisions in a distribution contract during the fourth quarter of 1993. Operating expenses which consist of research and development, sales and marketing, distribution, general and administrative and royalty expenses decreased significantly in the 10 week period ended December 31, 1994 compared with the fourth quarter of 1993. The primary reasons for the decrease are the two week difference in the reporting period and the cost reductions resulting from the restructuring program implemented during the third quarter of 1994. These combined with severance costs related to technology changes recorded during the fourth quarter of 1993 account for the decrease. Amortization of intangible assets was reduced from the full quarter 1993 levels due to the two week difference in the reporting periods. Interest expense increased significantly during the 10 week period ended December 31, 1994 as compared with the quarter ended December 31, 1993. This reflects the higher amount outstanding on the revolving line of credit during 1994 combined with increasing interest rates. Other expense for the 10 week period ended December 31, 1994 was less than the full quarter ended December 31, 1993 primarily because 1993 was impacted by the $330 write off of obsolete equipment due to the introduction of new technology and the valuation reserve established to write off a $251 investment in a patient care business which occurred during the fourth quarter of 1993. Under "fresh start" accounting for financial reporting purposes in accordance with the American Institute of Certified Public Accountants Statement of Position 90-7 and current accounting for income tax rules, utilization of the NOL carryforwards are required to offset intangible assets and do not offset income tax expense. Therefore, a federal income tax provision has been appropriately recorded for the 10 week period ended December 31, 1994. Results of Continuing Operations for the 42 Week Period Ended October 14, 1994 and for the Year Ended December 31, 1993 and for the Year Ended December 31, 1994 on a Pro Forma Basis: The following analysis compares the 42 week period ended October 14, 1994 to the year ended December 31, 1993. Due to the difference in the length of the reporting periods the results for the two periods are not directly comparable. PRO FORMA CONSOLIDATED (In Thousands)
For the For the For the 42 Weeks Year Year Ended Ended Ended October 14, December 31, December 31, 1994 1993 1994 -------- -------- -------- Revenues ........................... $ 24,882 $ 33,281 $ 32,280 Cost of sales ...................... 14,617 19,151 18,903 Operating expenses ................. 12,531 12,668 14,900 Amortization of intangible assets ................. 587 742 744 Interest expense ................... 370 277 496 Interest income .................... 15 74 21 Other expense, net ................. 159 345 152 Provision for income taxes ......... 0 0 221 -------- -------- -------- Net income (loss) .................. $ (3,366) $ 172 $ (3,114) ======== ======== ========
Revenues consist of NDM's patient care products (wound dressing, footpumps and related products) and critical care products (EKG electrodes, cables, leadwires and operating room products). Revenues for the 42 week period ended October 14, 1994 were less than the full year period ended December 31, 1993 primarily because of the ten week difference in the reporting periods. NDM anticipates that 1994 revenues for a comparable full year period would decrease approximately 3% from 1993 levels. Both patient care and critical care product revenues were adversely impacted by an inventory reduction program implemented by NDM's primary distributor as well as the acquisition of Hospital Supply Corporation of America, a hospital buying group and significant NDM customer, by the Columbia Healthcare System, which is not a customer of NDM. In addition, critical care product revenue was adversely affected by the introduction of a new line of products which initially experienced transition difficulties. NDM believes that it has resolved the issues associated with this product and that market acceptance has improved. Cost of sales decreased due to the ten week difference in the reporting periods. However, NDM estimates that, on a comparable full year basis, cost of sales would remain approximately even with 1993 even though: (a) revenues declined; (b) the Company implemented various manufacturing cost reductions throughout late 1993 and 1994; and (c) the Company settled certain provisions in a distribution contract favorably. These effects were offset by the writeoff of $603,000 of excess and obsolete inventory during the 42 week period ended October 14, 1994 due to new product introductions during this period in both critical care and patient care product groups. Also, cost of sales increased as a percentage of sales because the Company recorded a $192,000 accrual for rework costs related to critical care products during 1994. Operating expenses, which consist of research and development, sales and marketing, distribution, general and administrative and royalty expenses, for the 42 week period ended October 14, 1994 only decreased 1.1% compared to such costs for the full year ended December 31, 1993. This resulted from increased sales and marketing expenses of $1.3 million related to new product introductions, filling sales management positions that were open during 1993 and introducing new sales territories during 1994. The Company also experienced an increase in costs being charged for distribution by its primary distributor throughout 1994. Operating expenses also increased due to an increase in reserves for doubtful accounts receivable of $500,000 as a result of a deterioration in the aging of the account receivable, and an additional accrual for anticipated legal costs associated with patent defense of $300,000 which were recorded during 1994. Restructuring costs, consisting primarily of severance and outplacement costs, of $832,000 were incurred during 1994 compared with similar costs of $342,000 during 1993. Amortization of intangible assets decreased proportionately from the full year-1993 levels due to the ten week difference in the reporting periods. Interest expense increased significantly during the 42 week period ended October 14, 1994 as compared with the year ended December 31, 1993. This reflects the higher amount outstanding on the revolving line of credit during 1994 combined with higher interest rates (1994 effective rate of 7.28%). Interest income decreased during 1994 due to lower average cash balances combined with the ten week difference in the reporting periods. Other expense for the 42 week period ended October 14, 1994 was less than the full year 1993 primarily because 1993 was impacted by the write off of equipment obsolete due to the introduction of new technology and the valuation reserve established to write off an investment in a patient care business. Results of Continuing Operations on a Historical Basis for the Years Ended December 31, 1993 and 1992
Years Ended December 31, ------------------------ % 1993 1992 Change -------- -------- ------- (In Thousands) Revenues .............................. $ 33,281 $ 32,766 1.6% Cost of sales ......................... 19,277 17,824 8.2% Operating expenses .................... 12,648 11,224 12.7% Corporate general and administrative expenses .............. 2,500 3,405 -26.5% Amortization of intangible assets .................... 1,228 1,166 5.3% Interest expense ...................... 1,897 11,380 -83.3% Interest income ....................... 239 4,210 -94.3% Gain on sale of nonoperating assets .................. 0 1,144 N.M. Gain (loss) on marketable securities ........................... (700) 208 N.M. Other expense ......................... 768 331 132.0% Professional fees ..................... 5,883 0 N.M. Interest earned on accumulated cash ..................... 100 0 N.M.
The Company's revenues from continuing operations represent NDM's patient care and critical care products as follows:
Years Ended December 31, ------------------------ % 1993 1992 Change ------- ------- ------ (In Thousands) Critical care products ............. $29,969 $31,380 (4.5)% Patient care products .............. 3,312 1,386 139.0% ------- ------- ----- TOTAL REVENUES ..................... $33,281 $32,766 1.6% ======= ======= =====
Revenues were essentially flat for the periods due to the fact that NDM's primary critical care products have become mature and are now more price driven than in prior years. In 1993, NDM experienced a 4.5% decrease in the critical care product revenues, when compared to 1992, which management attributes to price erosion and volume decreases reflecting lower year-end sales to NDM's major distributor in 1993. The patient care product revenues increased 139% in 1993 compared with 1992. The 1993 increase resulted from volume increases combined with new product introductions. NDM attributes the significant increase primarily to wound dressing revenues which increased as a result of the advantages of Clearsite's hydrogel technology, NDM's sales force being allowed to sell Clearsite in the hospital and alternate site markets beginning in 1992 and NDM's ability to ship product under new foreign distribution agreements to Germany and Belgium in 1992 with further expansion to other foreign markets during 1993. NDM's cost of sales increased as a percentage of sales during 1993 when compared with 1992. This percentage increase was attributed to an increase in inventory reserves for obsolescence, increased start-up costs of new product introductions combined with sales price erosion in the critical care product line. Operating expenses, which consist of research and development, sales and marketing, distribution, general and administrative and royalty expenses increased 12.7% during 1993 as compared with 1992. Sales and marketing costs between years increased $852,000 which reflects the cost of additional sales representatives together with marketing expenses related to the start-up of new products and increased spending in tradeshows and periodicals. NDM's distribution costs, including warehousing, decreased by $115,000 in 1993 compared with 1992, due to a decreased distribution rate for non-exclusive accounts and lower product sales through its principal distributor. Research and development costs increased $151,000 primarily due to increased level of clinical studies and new product introductions. Operating general and administrative expenses increased $536,000 in 1993 over 1992 which was primarily due to a restructuring charge of $342,000 recorded during 1993. Corporate general and administrative expenses decreased in 1993 when compared with 1992 due principally to the MEI Diversified Chapter 11 bankruptcy which resulted in decreased legal expenses and lower salaries and wages as a result of staff reductions and executive salary reductions. Amortization expense increased in 1993 over 1992 and related to new patent amortization and increased goodwill relative to an acquisition made in late 1992. Interest expense in 1993 was down significantly due to the Chapter 11 filing of the Company and its domestic United States professional beauty salon subsidiaries, which ended the accrual of interest on all debt considered as a pre-petition liability subject to compromise. Interest income decreased significantly in 1993 as compared to 1992 due principally to lower cash and cash equivalent balances as cash was utilized in the professional beauty salon business together with lower short-term interest rates in 1993 relative to 1992. Gain on sale of nonoperating assets in 1992 represents a gain on the sale of certain nonoperating real estate together with a gain on the sale of the Company's aircraft charter subsidiary in the fourth quarter of 1992. The 1993 loss on marketable securities represented the decline in market value of Regis Corporation (Regis) common stock between December 16, 1993 and year end. See Note 4 of notes to the MEI Diversified consolidated financial statements. The 1992 gain on sale of marketable securities resulted from the March 1992 sale of a common stock investment. Other expense, net, in all periods represents the net operations of the other subsidiaries which are not significant. Professional fees incurred during 1993 represent reorganization costs incurred as a result of the Chapter 11 filing. Discontinued Operations On May 1, 1992, MEI Diversified sold the remaining net assets of its snack food segment. The segment's net operating results have been reported separately as discontinued operations in the accompanying MEI Diversified consolidated statements of operations for all years presented. See Note 3 of notes to the MEI Diversified consolidated financial statements. The gain on disposal of discontinued operations in the year 1992 represents the May 1992 sale of the net assets of the snack food segment. The 1992 loss from operations of the snack food segment included in loss from discontinued operations represents the related operating loss of the segment together with a realization provision for certain receivable and nonoperating real estate related to the sold snack food subsidiaries. The 1993 loss from operations of the discontinued snack food segment represents a realization provision for certain receivables and nonoperating real estate related to discontinued snack food subsidiaries. As mentioned above, in December 1993 MEI Diversified sold substantially all of the net assets of the professional beauty salon segment to Magicuts, Inc. The 1993 loss from operations of the discontinued professional beauty salon segment represents the salon operating losses prior to the formulation of a plan in June 1993 to sell the salon assets. The larger loss from discontinued operations in 1992 represents the substantial operating losses incurred by MEI Diversified in its professional beauty salon operations. The loss from the discontinued operations of the professional beauty salon segment includes a provision as of December 31, 1992 for disposal of net assets, sold in December 1993, at their net realizable value. The 1993 loss on the disposal of discontinued operations primarily represents the estimated salon operating losses expected to result from the date MEI Diversified began offering the segment for sale in June 1993 through the December 1993 sale date. The gain on settlement of Regis litigation represents the net value received in December 1993 on the Regis litigation referred to above which was settled as a part of the sale of the net assets of the professional beauty salon segment. Net Loss and Net Loss Per Common Share The 1993 net loss is due primarily to the operating loss from continued operations together with professional fees relative to the Chapter 11 reorganization and the operating loss and loss on disposition of the discontinued professional beauty salon segment offset in part by the gain on settlement of the Regis litigation in December 1993. The 1992 net loss is due principally to the professional beauty salon segment operating loss, the provision for disposal of the discontinued professional beauty salon segment and interest expense offset in part by the May 1992 gain on disposal of the snack food segment and interest income. Financial Condition as of December 31, 1994 As stated above, the Plan of Reorganization became effective on October 14, 1994. Under the Plan of Reorganization, Old NDM was merged into MEI Diversified, and MEI Diversified restated its Certificate of Incorporation and changed its name to New Dimensions In Medicine, Inc. Pursuant to the Plan of Reorganization, all assets and liabilities of MEI Diversified were distributed to certain liquidating estates established under the Plan of Reorganization, except for certain tax attributes of MEI Diversified and the capital stock of certain nonoperating subsidiaries. As a result of the merger, all assets and liabilities of Old NDM became assets and liabilities of the Company except that all obligations and liabilities owed by Old NDM to MEI Diversified were canceled pursuant to the Plan of Reorganization. The Company's Amended and Restated Certificate of Incorporation provides authorization for 20,000,000 shares of common stock. As of March 31, 1995, a total of 4,311,977 shares of Common Stock of NDM have been issued to certain creditors of MEI Diversified, including the holders of the 12-1/2% Senior Subordinated Notes of MEI Diversified due December 1, 1996 in the original principal amount of $75,000,000 and the 8% Convertible Debentures of MEI Diversified due December 1, 2006 in the original principal amount of $50,000,000 in partial satisfaction of their claims. The Company will issue a total of 4,500,000 shares of Common Stock to such creditors initially. As of March 29, 1995, 4,311,977 shares of Common Stock have been issued to such creditors. A total of 500,000 shares of Common Stock will be reserved for issuance to satisfy claims being made by certain former creditors of MEI Diversified to which the trust administrator established under the Plan of Reorganization is objecting. To the extent that these claims are denied, additional shares of Common Stock will not be issued. The allowed claim of each such creditor of MEI Diversified will be reduced by $7.60 for each share of Common Stock of NDM distributed to such creditors. The assets and liabilities of NDM were adjusted to their estimated fair market values as of October 15, 1994 in accordance with accounting principles for entities emerging from bankruptcy ("fresh-start reporting"). The valuation methodologies used to determine the reorganization value of NDM included an income capitalization approach, a cost approach and a sales comparison approach. Property, plant and equipment were valued using a combination of the cost approach and sales comparison approach. Intangible assets were valued using a combination of the cost approach and income capitalization approach. The estimated unleveraged reorganization value of NDM was computed using a discounted net cash flow technique utilizing an income capitalization approach. This specific technique takes into consideration (a) the discounted free cash flows generated by NDM through 1999, (b) the discounted residual value of NDM at the end of 1999 and (c) projected excess cash on hand at October 15, 1994. For purposes of discounting values, a weighted average cost of capital rate of 16.5% was utilized throughout the analysis. On the effective date of the Plan of Reorganization, all of the claims against MEI Diversified were released and discharged and became claims against the MEI Liquidating Estates established under the Plan of Reorganization. NDM's net working capital is $3.5 million at December 31, 1994. The Plan or Reorganization includes a provision whereby the trust administrator for the MEI Diversified Liquidating Trust will distribute up to $2 million to NDM to assist with NDM's need for additional working capital. As of December 31, 1994, NDM had received $1,742,000 of this amount, and as of January 9, 1995 NDM had received the full amount. Although the Company believes, based on its current plan, that it has sufficient working capital to maintain operations, if the Company does not meet its plan with respect to revenues or if expenses are higher than anticipated, the Company may not have sufficient working capital to continue operations. As of December 31, 1994, NDM had an outstanding balance of $2.5 million under a line of credit agreement with a commercial bank (the maximum amount permitted under the line of credit). The lender has a first security interest in substantially all of NDM's assets. The interest rate on the line of credit is one percent over the prime rate effective December 1, 1994. NDM's debt obligations include a floating rate option note with an outstanding balance of $6.0 million due in semi-annual installments of $400,000 which commenced on November 1, 1992 and matures May 1, 2002. The lender sets the interest rate on a weekly basis based on market conditions for similar debt. This rate was 6.28% at December 31, 1994 and 5.18% at October 15, 1994. The floating rate option note is cross collateralized and has a cross-default provision with respect to the line of credit. As a result of MEI Diversified Chapter 11 bankruptcy, Old NDM was in default under its line of credit and the floating rate option note. This default was cured on October 14, 1994 as a result of the Plan of Reorganization becoming effective. In addition, NDM had not been in compliance with certain financial covenants established while Old NDM was a subsidiary of MEI Diversified. NDM and its commercial bank have amended the loan agreement to provide financing at the same borrowing capacity through June 30, 1995. The financing arrangements contain various covenants related to cash flow, debt to equity ratio, current ratio, capital expenditures and tangible net worth, and the Company is in compliance with these covenants. As of December 31, 1994, the Company did not have any material commitments for capital expenditures. NDM's viability as a going concern is dependent on its ability to obtain long term financing and to maintain its return to profitability. Based on current trends and changes implemented in the third quarter of 1994, NDM expects its future operating expenses to decrease primarily due to: (a) cost savings from the third quarter restructuring, (b) no anticipated excess or obsolete inventory write offs, significant warranty claims, additional accruals for legal costs and significant provisions for potentially uncollectible accounts receivable, and (c) the elimination of MEI corporate general and administrative expenses. Management has prepared cash projections which are based on budgeted sales. Management believes cash plans will be adequate to fund future operations. Ultimately, NDM's ability to maintain operations will depend on the success of the restructuring implemented during the third quarter of 1994 which is intended to improve NDM's profitability. NDM's fourth quarter 1994 performance reflected the improvement from the third quarter restructuring as well as an increase in revenues compared with the third quarter of 1994. While the fourth quarter 1994 revenues and financial performance are a significant improvement over the third quarter 1994 results, there can be no assurance that NDM will be able to consistently achieve successful future operations. Item 8. FINANCIAL STATEMENTS AND SUPPLEMENTARY DATA. The Company's Consolidated Financial Statements and the reports of its independent auditors are included on pages F-1 to F-39 of this Annual Report. Item 9. CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS ON ACCOUNTING AND FINANCIAL DISCLOSURE. Not Applicable. PART III Item 10. DIRECTORS AND EXECUTIVE OFFICERS OF THE REGISTRANT. (a) Directors and Executive Officers The executive officers and directors of the Company, their ages and the offices held, as of March 15, 1995, are as follows:
Name Age Position in the Company - ---- --- ----------------------- William F. Shea 44 Chairman of the Board, Chief Executive Officer, President and Director James V. Cartmell 56 Vice President of Research and Development Philip J. Oliver 39 Vice President of Finance, Chief Financial Officer and Assistant Secretary Steven F. Glover 40 Vice President of Sales Thomas A. Cycyota 36 Vice President of Marketing David K. Snider 45 Vice President of Business Development David J. Brail 30 Director Marc A. Gineris 36 Director Leigh Walzer 34 Director Thomas A. Letscher 34 Secretary
Information regarding the business experience of the executive officers of the Company is set forth below. William F. Shea. Mr. Shea became the Chairman of the Board, Chief Executive Officer, President and a Director of the Company following the effectiveness of the Plan of Reorganization. Prior to that time, he had been the President of Old NDM since January 1993 and had been the Vice President/General Manager of Old NDM from 1990 to January 1993. Prior to joining Old NDM, Mr. Shea served 16 years with The Kendall Company, including five years as General Manager of its operations in Japan. Mr. Shea received his Bachelor of Arts Degree in Economics from the College of the Holy Cross and his Masters of Business Administration from Boston University. James V. Cartmell. Mr. Cartmell became the Vice President of Research and Development of the Company following the effectiveness of the Plan of Reorganization, a position he had held with Old NDM. Mr. Cartmell had been employed by Old NDM since October 1972. Mr. Cartmell has also served as Director of Research and Development, Scientist and Manager of Clinical Testing of Old NDM. Mr. Cartmell holds numerous patents utilized in NDM's operations and has received the IR-100 Award two times. Prior to joining NDM, Mr. Cartmell was employed with the National Cash Register Co. and Monsanto Chemical Co. Mr. Cartmell received his Associate Degree in Chemical Technology and Bachelor's Degree in Chemistry from the University of Dayton. Philip J. Oliver. Mr. Oliver became the Vice President of Finance, Chief Financial Officer and Assistant Secretary of the Company following the effectiveness of the Plan of Reorganization. Prior to that time, he had been Vice President of Finance of Old NDM since January 1993 and Controller of Old NDM from September 1987 to January 1993. Prior to joining Old NDM, Mr. Oliver served as Manager of Cost Accounting and General Accounting for Liebel Flarsheim Co. and as an Internal Auditor for Sybron Corporation. Following graduation from Ithaca College with a Bachelor of Science Degree in Accounting, Mr. Oliver served on the audit staff with the independent public accounting firm of Deloitte Haskins and Sells (now Deloitte & Touche) for two years. Steven F. Glover. Mr. Glover became the Vice President of Sales of the Company following the effectiveness of the Plan of Reorganization. He had been Director of Sales of Old NDM since February 1991. Prior to that time, Mr. Glover had served in various sales management positions with Baxter Healthcare Corporation and Medical Networks Inc. Mr. Glover originally joined Old NDM in 1976 and had been employed by Old NDM for six years in various capacities, including Region Sales Manager, Sales Representative and Sales Administrator. Mr. Glover received his Bachelor of Arts Degree in Communication Arts from the University of Dayton and his Masters in Business Administration from Xavier University. Thomas A. Cycyota. Mr. Cycyota became the Vice President of Marketing of the Company following the effectiveness of the Plan of Reorganization. He had been Group Director of Marketing of Old NDM since November 1991. Prior to joining Old NDM, Mr. Cycyota served in various product and sales management positions with Kendall Healthcare Products Co., the most recent of which was Product Manager of their Wound Care Product Line. Mr. Cycyota received his Bachelor of Science Degree in Biology from the University of Illinois and his Masters in Business Administration in Finance from Loyola University. David K. Snider. Mr. Snider became the Vice President of Business Development of the Company following the effectiveness of the Plan of Reorganization. He had been Director of Marketing, O.R. Products of Old NDM since April 1992. Mr. Snider previously held positions in marketing management with Abiomed Cardiovascular, Inc., Becton Dickinson and Valleylab, Inc. Mr. Snider also served in the U.S. Air Force where he became a Registered Nurse and received his Bachelor of Science Degree from the Community College of the Air Force. David J. Brail. Mr. Brail became a Director of the Company upon the effectiveness of the Plan of Reorganization. Mr. Brail is a Vice President of, and head of research at, Dickstein Partners Inc., a New York investment firm which manages three investment funds, Dickstein & Co., L.P., Dickstein International Limited and Dickstein Focus Fund L.P. See "Principal and Selling Stockholders." Dickstein Partners Inc. is a principal stockholder of the Company. Mr. Brail also serves on the board of directors of Amerihost Properties, Inc. and Banyan Strategic Land Fund II. Prior to joining Dickstein Partners Inc. in 1987, Mr. Brail worked in corporate finance at Janney Montgomery Scott, Inc. He received a Bachelor of Science in Economics from the Wharton School at the University of Pennsylvania in 1987. Marc A. Gineris. Mr. Gineris became a Director of the Company upon the effectiveness of the Plan of Reorganization. Mr. Gineris is a Principal with Alex. Brown & Sons Incorporated, an investment banking firm. Alex. Brown was the financial advisor to the Creditors' Committee, which was dissolved upon effectiveness of the Plan of Reorganization. For the past ten years, Mr. Gineris has specialized in advising restructuring clients and executing leveraged buyout transactions. Prior to joining Alex. Brown in 1990, Mr. Gineris held positions with several lending investment banking firms in the Restructuring, Mergers and Acquisitions and Corporate Finance Departments. Mr. Gineris is also a member of the board of directors of Aileen, Inc., a New York Stock Exchange publicly traded company. Mr. Gineris holds a Masters in Business Administration from Harvard University and a Bachelor of Arts from Pomona College in Claremont, California. Leigh Walzer. Mr. Walzer was elected a Director of the Company on October 17, 1994 following the effectiveness of the Plan of Reorganization. Since June 1993, Mr. Walzer has been an analyst employed by Heine Securities Corporation. From April 1992 to June 1993, Mr. Walzer served as Senior Vice President of Jefferies & Co. From September 1991 to April 1992, Mr. Walzer was Vice President of BDS Securities, and, from October 1987 to September 1991, he was an analyst at Smith Management Co. (an affiliate BDS Securities in September 1991). Mr. Walzer holds a Masters in Business Administration from Harvard University and a Bachelor of Arts from Princeton University. Thomas A. Letscher. Mr. Letscher has been the Secretary of the Company since October 1994. He is a partner with the law firm of Oppenheimer Wolff & Donnelly, Minneapolis, Minnesota, where he has practiced since 1987. Mr. Letscher received his law degree from the University of California, Berkeley, and a Bachelor of Science in Engineering from the University of Wisconsin. The Current Board of Directors was elected following the effectiveness of the Plan of Reorganization. William F. Shea, David J. Brail and Marc A. Gineris were elected pursuant to the Plan of Reorganization, and Leigh Walzer was elected by these Board members at the first meeting of the Board of Directors following the effectiveness of the Plan of Reorganization, which was held on October 17, 1994. Generally, directors may be removed at any time, with or without cause, by the holders of a majority of the Company's Common Stock, except that within the earlier of the next annual meeting of stockholders or October 14, 1995, a director may only be removed for cause and only with the affirmative vote of a majority of the Company's outstanding Common Stock. Officers of the Company serve at the pleasure of the Board of Directors. The Company reimburses officers and directors for their authorized expenses. The Board of Directors has established an Audit Committee and a Compensation Committee. The Audit Committee provides assistance to the Board in satisfying its fiduciary responsibilities relating to accounting, auditing, operating and reporting practices of the Company. The Audit Committee reviews the annual financial statements of the Company, the selection and work of the Company's independent auditors and the adequacy of internal controls for compliance with corporate policies and directives. This committee currently consists of David J. Brail, Chair, Leigh Walzer and Marc A. Gineris. The Compensation Committee reviews and approves the general compensation and benefit programs of the Company and the specific compensation and benefits to be paid to the Company's executive officers. This committee currently consists of Leigh Walzer, Chair, David J. Brail and Marc A. Gineris. (b) Compliance with Section 16(a) of the Exchange Act Section 16(a) of the Securities Exchange Act of 1934, as amended (the "Exchange Act"), requires the Company's directors and executive officers and all persons who beneficially own more than 10% of the outstanding shares of the Company's Common Stock to file with the Securities and Exchange Commission initial reports of ownership and reports of changes in ownership of the Company's Common Stock. Executive officers, directors and greater than 10% beneficial owners are also required to furnish the Company with copies of all Section 16(a) forms they file. As part of the Plan of Reorganization, the former officers of Old NDM became the officers of the Company. None of these individuals have ever been officers, directors, or employees of MEI Diversified. In addition, none of the former officers or directors of MEI Diversified are officers, directors or employees of the Company. Accordingly, none of the current officers of the Company have any personal knowledge of the Section 16(a) forms filed, or required to be filed, by the former officers and directors of MEI Diversified. To the Company's knowledge, during the year ended December 31, 1994, all of the Company's directors, executive officers and beneficial owners of greater than 10% of the Company's Common Stock filed on a timely basis the forms required by Section 16 of the Exchange Act. Item 11. EXECUTIVE COMPENSATION. The following table sets forth for each of the last three fiscal years the compensation awarded to or earned by (a) the Chief Executive Officer of the Company and each of the four most highly compensated executive officers of the Company whose compensation exceeded $100,000 in 1994; and (b) the compensation awarded to or earned by the Chief Executive Officer of MEI Diversified.
Summary Compensation Table Annual Compensation ------------------------------------------------ Name and Fiscal Other Annual All Other Principal Position Year Salary Bonus Compensation Compensation ------------------ ------ ------ ----- ------------ ------------ William F. Shea(1)........ 1994 $230,000 $ 0 -- $ 1,925 President and Chief Executive 1993 $160,077 34,000 -- 2,024 Officer..................... 1992 $144,711 52,000 -- 41,112 James V. Cartmell(1)...... 1994 $135,000 0 -- 1,925 Vice President of........... 1993 $107,545 16,800 -- 1,873 Research and Development 1992 $ 97,396 23,914 -- 1,818 Philip J. Oliver(1)....... 1994 $115,000 0 -- 2,552 Vice President of Finance 1993 $ 85,800 16,300 -- 2,145 and CFO..................... 1992 $ 78,933 15,554 -- 2,917 Thomas A. Cycyota(1)...... 1994 $120,000 0 -- 2,310 Vice President of Marketing 1993 $ 87,731 16,800 -- 20,749 ............................ 1992 $ 78,966 17,250 -- 116,180 Steven F. Glover(1) ...... 1994 $130,000 0 -- 2,310 Vice President of Sales..... 1993 $ 95,077 17,300 -- 2,295 ............................ 1992 $ 91,057 22,500 -- 4,188 Donald E. Benson(2)....... 1994 $265,822 -- -- $ 3,712 President/Chief Executive 1993 $313,012 -- $1,500 $ 7,020 Officer..................... 1992 $400,230 -- $6,000 $ 7,020
- --------------- (1) Current executive officer of NDM. (2) Former executive officer of MEI Diversified. Executive Compensation Arrangements In October 1994, the Compensation Committee of the Board approved an annual base salary of $230,000 for William Shea, the Company's Chief Executive Officer, and annual base salaries between $115,000 and $135,000 for the other executive officers. In March 1995, the Compensation Committee approved the principle terms of a compensation plan for the Company's executive officers. This plan provides for the base salaries approved in October 1994. In the event of certain extraordinary corporate events, the plan provides for lump sum severance benefits equal to 24 months base salary, in the case of the Chief Executive Officer, and 18 months base salary, in the case of the other executive officers, as well as health insurance for the same periods. The Company is also obligated to pay the executive officers a cash payment equal to a percentage of the approximate proceeds to shareholders if certain extraordinary corporate events occur before December 31, 1995. The plan also provides for the grant of stock and stock options, which would vest at certain times after December 31, 1995 if no such extraordinary corporate events occur before before that time. Option Grants and Exercises in 1994 The Company did not grant options to any of the named executive officers in the fiscal year ended December 31, 1994 and, as of such date, none of the name executive officers held any options to purchase shares of common stock. Compensation Committee Report on Executive Compensation At the first meeting of the new Board of Directors following the effective date of the Plan of Reorganization, which was held on October 17, 1994, the Board established the Compensation Committee. This Committee consists solely of the Company's three non-employee directors: Leigh Walzer (Chair), David J. Brail and Marc A. Gineris. The Committee's goal is to provide the Company's executive officers with total compensation packages that are appropriate for the officers of similar public companies in the Company's industry, consistent with the Company's financial condition and performance. The Committee also desires to align the goals and objectives of executive management with those of the Company's stockholders. In October 1994, the Compensation Committee approved an increase in base salaries for the Company's executive officers, which was made retroactive to January 1, 1994. These salaries were based upon a review of base salaries for executive officers of public companies in the Company's industry. In addition, the Compensation Committee determined that it was appropriate to make the increases retroactive because of time delays involved in the MEl Diversified bankruptcy and the delays in the confirmation of the Plan of Reorganization. During that time, the executive officers of NDM remained in their positions despite significant uncertainty regarding the future of NDM and their individual employment opportunities. The Committee decided not to pay bonuses in 1994 due to the Company's financial performance in 1994 and its financial condition at the end of the year. However, assuming the Company returns to profitability in 1995, the Compensation Committee may pay bonuses for 1995. Because the Company has been going through a transition period following the confirmation of the Plan of Reorganization, the Committee only recently approved a compensation plan for the Chief Executive Officer and the other executive officers of the Company, which is described above. COMPENSATION COMMITTEE Leigh Walzer (Chair) David Brail Marc Generis Compensation Committee Interlocks/Insider Participation None of the members of the Company's Compensation Committee of the Board (David J. Brail, Leigh Walzer and Marc A. Gineris) is or has been an officer or employee of the Company or any of its subsidiaries. In addition, there are no Compensation Committee interlocks between the Company and other entities involving NDM executive officers and NDM directors who serve as executive officers or directors of such entities. Director Compensation The Company currently pays its nonemployee directors a fee of $10,000 per year, plus $500 for each board meeting attended and $250 for each committee meeting attended. At the present time such director fees are paid on an annual basis in the form of shares of the Company's Common Stock. Any director compensation payable to Mr. Walzer will be distributed to the advisory clients of Heine Securities Corporation, which currently employs Mr. Walzer as an investment analyst. Comparative Stock Performance As of March 31, 1995, 4,311,977 shares of Common Stock were issued and outstanding. There is currently no established trading market. Pursuant to the Plan of Reorganization, the Company intends to submit an application for inclusion of the Common Stock on the National Association of Securities Dealers Automated Quotation ("NASDAQ") System. See "BUSINESS- Background." However, there can be no assurance that such application will be approved, and until such time the Company expects the Common Stock to be traded on local over-the-counter markets. Pension Plans Prior to the effective date of the Plan of Reorganization, MEI Diversified sponsored the MEI Diversified Inc. Pension Plan ("Diversified Plan"). Pursuant to the Plan of Reorganization, the Diversified Liquidating Trust has assumed the Diversified Plan and the Pension Benefit Guaranty Corporation has released any and all claims against NDM based upon the Diversified Plan. The following table reflects the estimated annual benefit under the Diversified Plan at retirement to persons at specified compensation levels at various years-of-service classification assumptions:
Defined Benefit Pension Table Years of Service Final Average ------------------------------------------------------------ Annual Earnings 10 15 20 25 --------------- -------- -------- --------- ----- $ 50,000 $ 7,800 $11,700 $15,600 $19,500 $ 75,000 12,300 18,500 24,600 30,800 $100,000 16,800 25,200 33,600 42,000 $125,000 21,300 32,000 42,600 53,300 $150,000 25,800 38,700 51,600 64,500 $175,000 30,300 45,500 60,600 75,800 $200,000 34,800 52,200 69,600 87,000 $225,000 39,300 59,000 78,600 98,300 $250,000 43,800 65,700 87,600 109,500
A participant having an accrued benefit under the terms of the Diversified Plan as in effect on December 31, 1988 will be entitled to the greater of such accrued benefit or the benefit stated in the above table, provided however, accrued benefits for highly compensated corporate headquarters employees (as defined in Section 414(q) of the Internal Revenue Code of 1954, as amended) (the "Code") are frozen at the level for such persons on December 31, 1988 or such later date as such an employee transferred to headquarters from another employer participating in the Diversified Plan. Except as to those persons for whom benefits accrued at a higher amount prior to January 1, 1983, annual benefits payable to participants under the Diversified Plan at age 65 may not exceed $112,221 pursuant to Section 415 of the Code. Compensation covered by the Diversified Plan includes basic and overtime pay, commissions and bonuses. Compensation is limited, adjusted for cost of living increases effective January 1, 1991 to $222,220, January 1, 1992 to $228,860, and January 1, 1993 to $235,840, and January 1, 1994 to $150,000. The compensation limitation is subject to further cost of living adjustments. All of the compensation in the table entitled "Summary Compensation Table," except that $235,840 in 1993 relating to Mr. Benson, is covered by the Diversified Plan. Mr. Benson has 25 credited years of service under the Diversified Plan as of October 14, 1994. An employee becomes a participant upon completion of certain age and service requirements. Monthly pension benefits are equal to 1.2% of a participant's final average monthly compensation (computed on the basis of the five (5) consecutive years out of the last ten (10) years which produces the highest average) plus .6% of his final average monthly compensation in excess of covered compensation multiplied by the participant's total years of benefit service to a maximum of 25 years. Covered compensation is the average (without indexing) of the social security taxable wage base in effect for each calendar year during the 35 year period ending with the calendar year in which the participant attains social security retirement age. Benefits are not subject to reduction for social security or offset by other amounts. According to the actuary for the Diversified Plan, the Diversified Plan is under-funded by approximately $520,000 on a termination basis, but is over-funded on an ongoing concern basis. Employer contributions may be required in the event that the assets in the Diversified Plan are insufficient to meet the annual minimum funding standards of Code section 412. An increase in interest rates may cause the Diversified Plan to become over-funded on a termination basis at a future date. A disability contract covers employees who were officers (including those who are directors), general managers and department heads of MEI Diversified's or its subsidiaries. It provides a disability benefit after a six-month waiting period, until age 65, of two-thirds of the employee's monthly salary to a maximum benefit of $3,500 per month, less the employee's primary Social Security benefit. Item 12. SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT. The following table sets forth certain information with respect to beneficial ownership of the Company's Common Stock as of March 15, 1995 (a) by each person who is known by the Company to beneficially own more than five percent of the Company's Common Stock, (b) by each of the Company's directors, (c) each of the Company's executive officers named in the Summary Compensation Table above, and (d) by all executive officers and directors of the Company as a group.
Number of Shares Percentage Name Beneficially Owned(1) Ownership(2) - ---- --------------------- ------------ Dickstein & Co., L.P.(3) c/o Dickstein Partners Inc. Suite 4630 9 West 57th Street New York, NY 10019...................... 340,265 7.6% Dickstein International Limited(3) c/o Dickstein Partners Inc. Suite 4630 9 West 57th Street New York, NY 10019...................... 72,015 1.6% Heine Securities Corporation(4) 51 John F. Kennedy Parkway Short Hills, New Jersey 07078............ 932,459 20.7% Executive Life Insurance Company of New York 123 William Street New York, NY 10038...................... 346,095 7.7% William F. Shea.......................... 0 0 James V. Cartmell........................ 0 0 Philip J. Oliver......................... 0 0 Thomas A. Cycyota........................ 0 0 Steven F. Glover......................... 0 0 Marc A. Gineris.......................... 0 0 David J. Brail(5)........................ 0 0 Leigh Walzer(6).......................... 0 0 All executive officers and directors as a group (9 persons)...................... 0 0
- ---------------------- (1) Shares not outstanding but deemed beneficially owned by virtue of the right of an individual or entity to acquire them within 60 days are treated as outstanding only when determining the amount and percentage owned by such individual or entity. (2) Unless otherwise noted, each person or group identified possesses sole voting and investment power with respect to the shares shown opposite the name of such person or group. (3) David J. Brail, a director of the Company, is Vice President of Dickstein Partners Inc. which is the General Partner of Dickstein & Co., L.P. and the advisor to Dickstein International Limited. (4) Leigh Walzer, a director of the Company, is an investment analyst employed by Heine Securities Corporation. (5) Does not include 340,265 shares of Common Stock and 72,015 shares of Common Stock beneficially owned by Dickstein & Co., L.P. and Dickstein International Limited, respectively. See Note 3 above. (6) Does not include 932,459 shares of Common Stock beneficially owned by Heine Securities Corporation. See Note 4 above. Item 13. CERTAIN RELATIONSHIPS AND RELATED TRANSACTIONS. Pursuant to the Plan of Reorganization, the Company became obligated under the Registration Rights Agreement, dated as of October 14, 1994, among the Company and the Selling Stockholders to prepare and file a registration statement under the Securities Act of 1933, to register the resale of certain shares of Common Stock held by such stockholders. The Company has not yet filed any such registration statement. Dickstein Partners Inc., is the general partner of Dickstein & Co., L.P. and advisor to Dickstein International Limited. David J. Brail, a director of the Company, is a Vice President of Dickstein Partners Inc. Mr. Brail also served as a member of the Official Committee of Unsecured Creditors for MEI Diversified, which was the proponent of the Plan of Reorganization. Leigh Walzer, a director of the Company, is employed by Heine Securities Corporation. PART IV Item EXHIBITS, FINANCIAL STATEMENT SCHEDULES AND REPORTS ON FORM 8-K. (a)(1) Financial Statements of Registrant For the period ended October 14, 1994, the ten weeks ended December 31, 1994 and the fiscal years ended December 31, 1993 and 1992 Page ---- MEI DIVERSIFIED INC. AND SUBSIDIARIES As of October 14, 1994 and December 31, 1993 and For the Period Ended October 14, 1994 and For Each of Two Years in the Period Ended December 31, 1993 Report of Independent Public Accountants ....................................F-3 Consolidated Balance Sheets .................................................F-5 Consolidated Statements of Operations .......................................F-6 Consolidated Statements of Stockholders' Equity (Deficit)....................F-7 Consolidated Statements of Cash Flows .......................................F-8 Notes to Consolidated Financial Statements...................................F-9 NEW DIMENSIONS IN MEDICINE, INC. AND SUBSIDIARIES As of December 31, 1994 and For the Ten Week Period Ending December 31, 1994 and October 15, 1994 Report of Independent Public Accountants....................................F-26 Consolidated Balance Sheets.................................................F-27 Consolidated Income Statement ..............................................F-28 Consolidated Statement of Stockholders' Equity .............................F-29 Consolidated Statement of Cash Flows........................................F-30 Notes to Consolidated Financial Statements..................................F-31 (a)(2) Financial Statement Schedules of Registrant The following supplemental schedules are included in this Annual Report on Form 10-K at the page numbers set forth below and should be read in conjunction with the Financial Statements referred to above: Page ---- MEI Diversified Inc. and Subsidiaries (Period Ended October 14, 1994) II - Valuation and Qualifying Accounts and Reserves ...............F-23 New Dimensions In Medicine, Inc. and Subsidiaries (Ten Weeks Ended December 31, 1994) II - Valuation and Qualifying Accounts and Reserves................F-42 All other schedules are omitted as the required information is inapplicable or the information is presented in the financial statements or related notes. (a)(3) Exhibits The Exhibits to this Annual Report are listed in the Exhibit Index on pages 88-90 of this Annual Report on Form 10-K. The following is a list of each management contract or compensatory plan or arrangement required to be filed as an Exhibit to this Annual Report on Form 10-K pursuant to Item 14(c): (1) Executive Severance Agreement, dated August 18, 1993, between NDM Acquisition Corp. and William Shea (filed herewith). (b) Reports on Form 8-K No reports on Form 8-K have been filed during the fourth quarter of the Company's fiscal year ending December 31, 1994. SIGNATURES Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the Registrant has duly caused this Report to be signed by the following persons on March 29, 1995 on its behalf by the undersigned, thereunto duly authorized. NEW DIMENSIONS IN MEDICINE, INC. By /s/ William F. Shea ----------------------------------- William F. Shea Chief Executive Officer and President (Principal Executive Officer) By /s/ Philip J. Oliver ----------------------------------- Philip J. Oliver Vice President of Finance and Chief Financial Officer (Principal Financial and Accounting Officer) Pursuant to the requirements of the Securities Exchange Act of 1934, this Report has been signed by the following persons on March 29, 1995 on behalf of the Company in the capacities indicated. Signature Title --------- ----- /s/ William F. Shea Chairman of the Board and Director - --------------------------- William F. Shea /s/ David J. Brail Director - --------------------------- David J. Brail /s/ Marc A. Gineris Director - --------------------------- Marc A. Gineris /s/ Leigh Walzer Director - --------------------------- Leigh Walzer SECURITIES AND EXCHANGE COMMISSION WASHINGTON, D.C. 20549 FORM 10-Q Quarterly Report Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 For Quarter Ended September 30, 1995 Commission File Number 0-25840 New Dimensions in Medicine, Inc. ------------------------------------------------------ (Exact name of registrant as specified in its charter) Delaware 41-1549475 - --------------------------------------------- ------------------- (State or other jurisdiction of incorporation (I.R.S. Employer or organization Identification No.) 3040 East River Road, Dayton, Ohio 45439 - ---------------------------------------- -------- (Address of principal executive offices) (Zip Code) (513) 294-1767 ---------------------------------------------------- (Registrant's telephone number, including area code) Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes [ X ] No [ ] Indicate by check mark whether the registrant has filed all documents and reports required to be filed by Section 12, 13 or 15(d) of the Securities Exchange Act of 1934 subsequent to the distribution of securities under a plan confirmed by a Court. Yes [ X ] No [ ] As of October 31, 1995 the issuer had 4,325,686 shares of common stock $.01 par value outstanding. NEW DIMENSIONS IN MEDICINE INC. INDEX PART I. FINANCIAL INFORMATION Item 1 - Financial Statements - - Consolidated Condensed Balance Sheets - September 30, 1995 and December 31, 1994 - - Consolidated Condensed Statements of Income - Three Months and Nine Months Ended September 30, 1995 and 1994 - - Consolidated Condensed Statements of Cash Flows - Nine Months Ended September 30, 1995 and 1994 - - Notes to Consolidated Condensed Financial Statements Item 2 - Management's Discussion and Analysis of Financial Condition and Results of Operations Part II. Other Information PART I. FINANCIAL INFORMATION NEW DIMENSIONS IN MEDICINE, INC. AND SUBSIDIARIES CONSOLIDATED CONDENSED BALANCE SHEETS
(In Thousands) -------------------------- September 30, 1995 December 31, (Unaudited) 1994* ------- ------- ASSETS CURRENT ASSETS: Cash and cash equivalents ........................... $ 1,977 $ 1,130 Receivables, net of allowance of $467 and $355 ...... 4,372 5,386 Receivables from Diversified Liquidating Trust ...... 40 361 Inventories ......................................... 7,376 6,712 Prepaid expenses and other current assets ........... 194 365 ------- ------- Total current assets ................................ 13,959 13,954 ------- ------- PROPERTY, PLANT AND EQUIPMENT, net ..................... 10,622 11,326 OTHER LONG-TERM ASSETS ................................. 534 464 INTANGIBLE ASSETS, net ................................. 8,148 8,681 ------- ------- Total assets ........................................ $33,263 $34,425 ======= ======= LIABILITIES AND STOCKHOLDERS' EQUITY CURRENT LIABILITIES: Notes payable and current maturities of long-term debt ................................. $ 4,505 $ 3,306 Accounts payable .................................... 1,632 3,373 Accrued compensation and benefits ................... 1,475 1,729 Other accrued liabilities ........................... 1,994 2,061 ------- ------- Total current liabilities ........................... 9,606 10,469 ------- ------- LONG-TERM DEBT, LESS CURRENT MATURITIES ................ 4,800 5,204 ------- ------- STOCKHOLDERS' EQUITY Common stock, $.01 par value: 20,000,000 shares authorized 4,325,686 shares issued .......................... 43 43 Additional paid-in capital .......................... 18,457 18,457 Retained earnings ................................... 357 252 ------- ------- Total stockholders' equity .......................... 18,857 18,752 ------- ------- Total liabilities and stockholders' equity .......... $33,263 $34,425 ======= =======
* Consolidated condensed from audited financial statements. The accompanying notes are an integral part of these consolidated condensed financial statements. NEW DIMENSIONS IN MEDICINE, INC. AND SUBSIDIARIES CONSOLIDATED CONDENSED STATEMENTS OF INCOME
UNAUDITED (In Thousands, except per share data) Three Months Ended Nine Months Ended September 30, September 30, ------------------------- ------------------------- Pro forma Pro forma (See page 9) (See page 9) 1995 1994 1995 1994 -------- -------- -------- -------- NET SALES ...................................... $ 7,200 $ 6,051 $ 23,034 $ 24,216 COST OF SALES .................................. $ 4,209 $ 4,410 13,116 14,068 -------- -------- -------- -------- Gross profit .......................... 2,991 1,641 9,918 10,148 ELLING, GENERAL AND ADMINISTRATIVE EXPENSES ..................... $ 3,256 $ 5,067 9,489 12,665 -------- -------- -------- -------- Income (loss) from operations ......... (265) (3,426) 429 (2,517) OTHER INCOME (EXPENSE) Interest expense, net ................. ($ 145) ($ 111) (424) (328) Other income (expense), net ........... $ 79 ($ 252) 272 (178) -------- -------- -------- -------- Income before provision for income taxes ....................... (331) (3,789) 277 (3,023) PROVISION FOR INCOME TAXES ..................... ($ 81) ($ 319) 173 0 -------- -------- -------- -------- NET INCOME (LOSS) .............................. ($ 250) ($ 3,470) $ 104 ($ 3,023) ======== ======== ======== ======== PRO FORMA WEIGHTED AVERAGE NUMBER OF SHARES OUTSTANDING ............................. 4,325 4,325 4,325 4,325 -------- -------- -------- -------- PRO FORMA NET INCOME (LOSS) PER SHARE .......... ($ 0.06) ($ 0.80) $ 0.02 ($ 0.70) ======== ======== ======== ========
The accompanying notes are an integral part of these consolidated condensed financial statements. NEW DIMENSIONS IN MEDICINE, INC. AND SUBSIDIARIES CONSOLIDATED CONDENSED STATEMENTS OF CASH FLOWS
Unaudited (In Thousands) ------------------------------- Nine Months Ended September 30, ------------------------------- Pro forma (See page 11) 1995 1994 ------- ------- OPERATING ACTIVITIES: Net income ..................................................... $ 104 ($3,023) Adjustments to reconcile net income to net cash provided by operating activities: Depreciation and amortization ................................ 1,558 1,551 Change in other current assets and liabilities: Receivables ............................................ 1,335 429 Inventories ............................................ (661) (2,042) Prepaid expenses and other current assets .............. 171 (51) Accounts payable ....................................... (1,741) 3,505 Accrued liabilities .................................... (321) 0 ------- ------- Net cash provided by (used in) operating activities 445 369 ------- ------- CASH FLOWS FROM INVESTING ACTIVITIES: Additions of property, plant and equipment ..................... (284) (1,536) Decrease (increase) in other long-term assets and intangibles .. (116) 169 Proceeds from sales of fixed assets ............................ 7 24 ------- ------- Cash provided by investing activities ......... (393) (1,343) ------- ------- CASH FLOWS FROM FINANCING ACTIVITIES: Distribution by MEI Diversified Liquidating Trust .............. 0 450 Borrowings under bank line of credit agreement ................. 1,200 0 Payment of long-term debt ...................................... (405) (404) ------- ------- Cash provided by financing activities ............. 795 46 ------- ------- Net increase (decrease) in cash and cash equivalent 847 (928) ------- ------- Cash and cash equivalents, beginning of period .................. 1,130 1,358 ======= ======= Cash and cash equivalents, end of period ........................ $ 1,977 $ 430 ======= =======
The accompanying notes are an integral part of these consolidated condensed financial statements. NEW DIMENSIONS IN MEDICINE, INC. AND SUBSIDIARIES NOTES TO CONSOLIDATED CONDENSED FINANCIAL STATEMENTS Note 1. Company Reorganization (a) Business New Dimensions in Medicine, Inc. (NDM, the Company) is a developer and manufacturer of electrocardiograph monitoring electrodes, electrosurgical products, circulatory aids and hydrogel wound dressings. The Company also purchases and resells other medical devices such as foot pumps and the associated accessories, generators and surgical tools. The Company is in a single line of business which includes two separate product lines. The majority of the Company's sales are to domestic customers. The Company formerly conducted its business under the name "NDM Acquisition Corp.," incorporated in Minnesota. (b) New Basis of Accounting - Fresh Start Reporting NDM Acquisition Corp. (Old NDM) was a wholly-owned subsidiary of MEI Diversified, Inc. (MEI), a Delaware corporation. On February 23, 1993, MEI filed a petition for relief under Chapter 11 of the United States Bankruptcy Code (the Bankruptcy Code or Chapter 11) in the district of Delaware federal bankruptcy court. Old NDM was not a named party in this filing. On October 14, 1994, (the Effective Date), MEI emerged from Chapter 11, pursuant to the Amended Plan of Reorganization (the Plan) of the Official Committee of Unsecured Creditors for MEI Diversified, Inc. et al, dated September 27, 1994, which was confirmed by the U.S. Bankruptcy Court on September 28, 1994. Under the Plan, Old NDM was merged into MEI, and MEI then restated its Certificate of Incorporation and changed its name to New Dimensions in Medicine, Inc. Pursuant to the Plan, all assets and liabilities of MEI were distributed to certain liquidating estates established under the Plan, except for certain tax attributes of MEI, the capital stock of certain non-operating subsidiaries and the capital stock of Old NDM. As a result of the merger, all assets and liabilities of Old NDM became assets and liabilities of the Company except that all obligations and liabilities owed by Old NDM to MEI or any of its subsidiaries or affiliates were canceled pursuant to the Plan. The Plan also included a provision whereby the trust administrator for the Diversified Liquidating Trust would distribute $2,000,000 plus payment of certain professional fees to assist with the Company's working capital requirements. As of September 30, 1995, the Company had received $2,176,000 and the accompanying consolidated condensed balance sheet reflects a receivable of $40,000. On the day after the Effective Date (October 15, 1994) the Company adopted American Institute of Certified Public Accountants Statement of Position 90-7, "Financial Reporting by Entities in Reorganization" ("SOP 90-7"). SOP 90-7 requires that the accompanying balance sheet be prepared on the basis that a new reporting entity has been created and that assets and liabilities should be recorded at their estimated fair values as of the Effective Date. This method of accounting is referred to as "fresh-start" reporting. In accordance with SOP 90-7, the provision for federal income taxes is treated as a reduction in the valuation allowance against the net operating losses that existed at the date of adoption of "fresh start" accounting and is credited against intangible assets. Estimated fair values were determined by management with the assistance of independent appraisers. The valuation methodologies employed to determine the reorganization value of the Company included an income capitalization approach, a cost approach, and a sales comparison approach. Property, plant and equipment were valued using a combination of the cost approach and sales comparison approach. Intangible assets were valued using a combination of the cost approach and income capitalization approach. The estimated unleveraged reorganization value of the Company was computed using a discounted net cash flow technique utilizing an income capitalization approach. This specific technique takes into consideration (i) the estimated discounted free cash flows generated by the Company through 1999 (ii) the estimated discounted residual value of the Company at the end of 1999, and (iii) projected excess cash on hand at the Effective Date. For purposes of discounting values, a weighted average cost of capital rate of 16.5% was utilized throughout the analysis. On the Effective Date, all of the claims against MEI were released and discharged pursuant to the Plan and became claims against the MEI Liquidating Estates. In addition, any and all defaults arising under contracts or agreements of Old NDM as a result of the merger of Old NDM into MEI under the Plan, or as a result of the distribution of Company stock to creditors as provided under the Plan, shall be unenforceable against the Company. As of September 30, 1995, the Company had issued 4,325,686 shares and may issue up to an additional 96,844 shares to certain former creditors of MEI. If any of these additional shares are issued, their issuance will have no effect on the Company's opening stockholders' equity balance. (c) Net Income Per Share For financial reporting purposes, net income per share has been computed on a pro forma basis using the weighted average number of shares assuming that all 4,325,686 shares issued under the Plan were outstanding as of the beginning of the period. Note 2. Asset Purchase Agreement On October 18, 1995, the Company and CONMED Corporation ("CONMED") entered into an Asset Purchase Agreement (the "Agreement"), pursuant to which CONMED will purchase substantially all of the Company's assets, except its hydrogel wound care business outside of the United States, Mexico and Canada and its foot pump business. CONMED will assume liabilities related to the assets being acquired. The purchase price for the assets is $32,134,299, subject to certain adjustments for the disposition of the excluded assets and satisfaction of liabilities related to the excluded assets. In addition, the purchase price will be adjusted if the Company's net assets, subject to certain adjustments for excluded assets and liabilities and depreciation and amortization, increase by more than $1,700,000 or decrease by more than $1,000,000 from August 31, 1995 through closing. CONMED is also obligated to enter into certain agreements with the purchaser of the Company's international wound care business. The consummation of the Agreement is subject to additional conditions including the approval of the shareholders of the Company and required regulatory approvals. Additionally, pursuant to a separate letter of intent agreement between the Company and a third party, the Company will sell the assets and technology of the international wound care business to the third party and is in the process of negotiating a definitive agreement. Following consummation of the above transactions, the Company intends to wind-down operations and liquidate its remaining assets. Additionally, the Company intends to distribute the net proceeds from the above discussed asset sales to its shareholders. The proposed CONMED transaction is subject to regulatory approvals and approval by the Company's shareholders. The Company has not recorded any adjustments to the carrying amounts of its assets and liabilities to adopt the liquidation basis of accounting or the contingencies that may be triggered by these transactions, such as the repayment of outstanding debt and severance liabilities. Under the liquidation basis of accounting, assets would be adjusted to their estimated realizable value and liabilities would be adjusted to their estimated settlement amount. Note 3. Basis of Presentation In the opinion of management, the accompanying unaudited consolidated condensed financial statements contain all adjustments (consisting of only normal recurring accruals) necessary to present fairly the consolidated financial position of New Dimensions in Medicine, Inc. and Subsidiaries as of September 30, 1995 and December 31, 1994, and the results of operations for the three and nine month periods ended September 30, 1995 and 1994 and cash flows for the nine month periods ended September 30, 1995 and 1994. The consolidated condensed financial statements have been prepared under the presumption that users of the interim financial information have either read or have access to the audited consolidated financial statements for the ten week period ending December 31, 1994. Accordingly, certain information and footnote disclosure which would substantially duplicate the disclosure contained in the audited financial statements has been omitted from these interim financial statements pursuant to the rules and regulations of the Securities and Exchange Commission. It is suggested that these interim consolidated condensed financial statements be read in conjunction with the consolidated financial statements and the notes thereto, included in the Company's latest annual report on Form 10-K. Note 4. Inventories Inventories are valued at the lower of cost (first-in, first-out) or market value. The following is a summary of the components of inventory at September 30, 1995 and December 31, 1994:
(In Thousands) ------------------------------------- September 30, 1995 (unaudited) December 31, 1994 ------------------ ----------------- Raw Materials .......................... $ 3,332 $ 2,911 Work-In-Process ........................ 95 37 Finished Goods ......................... 5,138 4,850 Inventory Reserves ..................... (1,189) (1,086) -------- -------- $ 7,376 $ 6,712 ======== ========
Note 5. Supplementary Cash Flow Information Supplementary cash flow information for the nine months ended September 30, 1995 and 1994 follows:
(In Thousands) ------------------------- 1994 1995 (Pro Forma) ---- ----------- Interest Paid ................................ $469 $343 ==== ==== Income Taxes Paid ............................ 61 0 ==== ====
Note 6. Unaudited Pro Forma Financial Information The unaudited pro forma statements of operations for the three and nine months ended September 30, 1994 and the pro forma statement of cash flows for the nine months ended September 30, 1994 give effect to the Plan of Reorganization as if it had occurred, and such transactions had been consummated as of January 1, 1994. The following unaudited pro forma financial information does not purport to represent what the Company's actual results of operations or cash flows would have been had the effective date in fact occurred, and had such transactions in fact been consummated, at the beginning of this period. The unaudited pro forma financial information does not give effect to any transactions other than those included in the Plan of Reorganization and those discussed in the accompanying Notes to Unaudited Pro Forma Financial Information, or to the Company's results of operations since October 15, 1994. The following financial information is based upon the historical financial statements of MEI Diversified, Inc. for the three and nine months ended September 30, 1994 and should be read in conjunction with such historical financial statements and notes. NEW DIMENSIONS IN MEDICINE, INC UNAUDITED PRO FORMA CONSOLIDATED STATEMENT OF OPERATIONS (IN THOUSANDS)
FOR THE THREE MONTHS ENDED SEPTEMBER 30, 1994 ------------------------------------------------- MEI NEW DIMENSIONS DIVERSIFIED, IN PRO FORMA IN MEDICINE, INC. HISTORICAL ADJUSTMENTS PRO FORMA ------------------------------------------------- REVENUES $6,051 $ 0 $6,051 COSTS AND EXPENSES: COST OF SALES 4,289 (147)(2) 268 (3) 4,410 OPERATING EXPENSES 5,283 67 (3) (36)(2) (460)(6) 31 (7) 4,885 CORPORATE GENERAL AND ADMINISTRATIVE EXPENSES 400 (400)(1) 0 AMORTIZATION OF INTANGIBLE ASSETS 256 (256)(4) ------------------------------------------------- TOTAL COST AND EXPENSES 10,228 (751) 9,477 OPERATING INCOME (LOSS) (4,177) 751 (3,426) INTEREST EXPENSE (139) 13 (1) (126) INTEREST INCOME 34 (30)(1) 4 OTHER (EXPENSE) INCOME, NET (6,095) 5,854 (1) (241) ------------------------------------------------- LOSS FROM CONTINUING OPERATIONS BEFORE INCOME TAXES AND REORGANIZATION ITEMS (10,377) 6,588 (3,789) REORGANIZATION ITEMS: PROFESSIONAL FEES (1,078) 1,078 (1) 0 INTEREST EARNED ON ACCUMULATED CASH 9 (9)(1) 0 ------------------------------------------------- INCOME / (LOSS) FROM CONTINUING OPERATIONS BEFORE INCOME TAXES (11,446) 7,657 (3,789) PROVISION FOR INCOME TAXES 0 319 (8) 319 ------------------------------------------------- INCOME / (LOSS) FROM CONTINUING OPERATIONS (11,446) 7,976 (3,470) DISCONTINUED OPERATIONS: DISCONTINUED OPERATIONS, NET OF INCOME TAXES 0 0 ------------------------------------------------- NET INCOME / (LOSS) ($11,446) $7,976 ($3,470) =================================================
(Continued) See Accompanying Notes to Unaudited Pro Forma Financial Information NEW DIMENSIONS IN MEDICINE, INC UNAUDITED PRO FORMA CONSOLIDATED STATEMENT OF OPERATIONS (Continued) (IN THOUSANDS)
FOR THE NINE MONTHS ENDED SEPTEMBER 30, 1994 ------------------------------------------------- MEI NEW DIMENSIONS DIVERSIFIED, IN PRO FORMA IN MEDICINE, INC. HISTORICAL ADJUSTMENTS PRO FORMA ------------------------------------------------- REVENUES $24,216 $ 0 $24,216 COSTS AND EXPENSES: COST OF SALES 14,103 (839)(2) 804 (3) 14,068 OPERATING EXPENSES 12,350 201 (3) (210)(2) (421)(6) 199 (7) 12,119 CORPORATE GENERAL AND ADMINISTRATIVE EXPENSES 1,179 (1,179)(1) 0 AMORTIZATION OF INTANGIBLE ASSETS 764 (764)(4) 546 (5) 546 ------------------------------------------------- TOTAL COST AND EXPENSES 28,396 (1,663) 26,733 OPERATING INCOME (LOSS) (4,180) 1,663 (2,517) INTEREST EXPENSE (350) 7 (1) (343) INTEREST INCOME 119 (104)(1) 15 OTHER (EXPENSE) INCOME, NET (6,576) 6,398 (1) (178) ------------------------------------------------- LOSS FROM CONTINUING OPERATIONS BEFORE INCOME TAXES AND REORGANIZATION ITEMS (10,987) 7,964 (3,023) REORGANIZATION ITEMS: PROFESSIONAL FEES (3,949) 3,949 (1) 0 INTEREST EARNED ON ACCUMULATED CASH 31 (31)(1) 0 ------------------------------------------------- INCOME / (LOSS) FROM CONTINUING OPERATIONS BEFORE INCOME TAXES (14,905) 11,882 (3,023) PROVISION FOR INCOME TAXES 0 0 (8) 0 ------------------------------------------------- INCOME / (LOSS) FROM CONTINUING OPERATIONS (14,905) 11,882 (3,023) DISCONTINUED OPERATIONS: DISCONTINUED OPERATIONS, NET OF INCOME TAXES 352 (352)(1) 0 ------------------------------------------------- NET INCOME / (LOSS) ($14,553) $11,530 ($3,023) =================================================
See Accompanying Notes to Unaudited Pro Forma Financial Information NOTES TO UNAUDITED PRO FORMA FINANCIAL INFORMATION UNAUDITED PRO FORMA CONSOLIDATED STATEMENTS OF OPERATIONS (1) To eliminate the profit and loss effect of former MEI Diversified Inc. subsidiaries as their assets and liabilities have been transferred into the various Liquidating Trusts established under the Plan of Reorganization. (2) To reverse the historical amortization of the excess of cost over fair value of assets acquired and of other intangible assets. (3) To record amortization expense based on the revised fair value of intangible assets (patents and trademarks). (4) To record depreciation expense based on the revised fair value basis of property, plant and equipment. (5) To reverse the historical depreciation on property, plant, and equipment. (6) To reverse the historical amortization expense of start up, marketing and regulatory costs incurred related to new product introductions. (7) To record start up, marketing and regulatory costs incurred related to new product introductions based on the revised fair value of these costs. (8) To record an appropriate tax provision for federal income and state franchise tax. NEW DIMENSIONS IN MEDICINE, INC UNAUDITED PRO FORMA CONSOLIDATED STATEMENT OF CASH FLOWS (IN THOUSANDS)
FOR THE NINE MONTHS ENDED SEPTEMBER 30, 1994 MEI NEW DIMENSIONS DIVERSIFIED, IN PRO FORMA IN MEDICINE, INC. HISTORICAL ADJUSTMENTS PRO FORMA ---------- ----------- --------- OPERATING ACTIVITIES: Net income ........................................................................... ($14,553) $ 11,530 ($ 3,023) Adjustments to reconcile net income to net cash provided by operating activities: Reserve for real estate write-down ................................................. 5,000 (5,000)(1) Depreciation and amortization ...................................................... 2,641 (828)(1) (1,049)(5) 1,005 (4) (764)(2) 546(3) 1,551 Other, net ......................................................................... 397 (397)(1) 0 Change in other current assets and liabilities: Receivables ........................................................................ 424 5 (1) 429 Inventories ........................................................................ (2,246) 204(1) (2,042) Prepaid expenses and other current assets .......................................... (48) (3)(1) (51) Accounts payable and accrued expenses .............................................. 3,660 (155)(1) 0 (6) 3,505 Pre-petition liabilities not subject to compromise ................................. (49) 49 (1) 0 Pre-petition liabilities subject to compromise ..................................... 446 (446)(1) 0 Net current assets of discontinued operations ...................................... 400 (400)(1) 0 -------- -------- -------- Net cash provided by (used for) operating activies ............................................................ (3,928) 4,297 369 -------- -------- -------- CASH FLOWS FROM INVESTING ACTIVITIES: Proceeds from sale of property ....................................................... 554 (530)(1) 24 Decrease in other long-term assets and intangibles ................................... 0 169 (1) 169 Additions of property, plant and equipment ........................................... (1,536) 0 (1) (1,536) -------- -------- -------- Cash used in investing activities ............................................... (982) (361) (1,343) -------- -------- -------- CASH FLOWS FROM FINANCING ACTIVITIES: Distribution by MEI Liquidating Trust ................................................ 0 450 450 Payment of long-term debt ............................................................ (404) 0 (404) -------- -------- -------- Cash used in financing activities ............................................... (404) 0 46 -------- -------- -------- Net increase in cash and cash equivalents ....................................... (5,314) 4,386 (1) (928) -------- -------- -------- Cash and cash equivalents, beginning of period ........................................ 8,106 (6,748) 1,358 -------- -------- -------- Cash and cash equivalents, end of period .............................................. $ 2,792 ($ 2,362) $ 430 ======== ======== ========
See Accompanying Notes to Unaudited Pro Forma Financial Information NOTES TO UNAUDITED PRO FORMA FINANCIAL INFORMATION UNAUDITED PRO FORMA CONSOLIDATED STATEMENT OF CASH FLOWS (1) To eliminate the cash flow effect of former MEI Diversified Inc. subsidiaries as their assets and liabilities have been transferred into the various Liquidating Trusts established under the Plan of Reorganization. (2) To reverse the historical amortization of the excess of cost over fair value of assets acquired and of other intangible assets. (3) To record amortization expense based on the revised fair value of intangible assets (patents and trademarks). (4) To record depreciation expense based on the revised fair value basis of property, plant and equipment. (5) To reverse the historical depreciation on property, plant, and equipment. (6) To record an appropriate tax provision for federal income tax and state franchise tax. MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS Results of Operations
Unaudited Unaudited Three Months Ended September 30, Nine Months Ended September 30, (Dollars In Thousands) (Dollars In Thousands) ----------------------------------------- ---------------------------------------- Pro Forma Pro Forma (See Page 9) % (See Page 9) % 1995 1994 Change 1995 1994 Change ------ ------- ------ ------- ------- ------ Revenues $7,200 $ 6,051 19.0% $23,034 $24,216 -4.9% Cost of Sales 4,209 4,410 -4.6% 13,116 14,068 -6.8% Operating Expenses 3,256 5,067 -35.7% 9,489 12,665 -25.1% Operating Income (loss) (265) (3,426) 92.3% 429 (2,517) 117.1% Interest Expense, net 145 122 18.9% 424 328 29.4% Other Income (expense) 79 (241) 132.8% 272 (178) 253.0% Income Tax Provision (benefit) (81) (319) 74.6% 173 0 N.M. Net Income (loss) (250) (3,470) 92.8% 104 (3,023) 103.5%
Revenue for the periods consisted of the following:
For the Three Months Ended For the Nine Months Ended September 30, (in thousands) September 30, (In Thousands) ---------------------------- ---------------------------- % % 1995 1994 Change 1995 1994 Change ---- ---- ------ ---- ---- ------ Critical Care Products $5,990 $5,269 13.7% $19,690 $21,583 -8.8% Patient Care Products 1,210 782 54.7% 3,344 2,633 27.0% ------ ------ ------- ------- Total Revenue $7,200 $6,051 19.0% $23,034 $24,216 -4.9% ====== ====== ======= =======
Revenues increased in the third quarter of 1995 by 19% compared to the third quarter of 1994 but decreased for the nine month period ended September 30, 1995 by 4.9% compared to the same period in 1994. Although revenues for the third quarter of 1995 increased from the third quarter of 1994, revenues for the third quarter of 1995 were below expectations in part due to the announcement of the sale of the Company's assets. Revenues from patient care products increased 54.7% in the third quarter and 27% for the nine month period compared to the same periods in 1994. The increase in patient care revenues during the third quarter included a 58.4% increase in wound care products and a 29.7% increase in the ActOne(a) foot pump products over the third quarter of 1994. The decrease in critical care product revenue for the nine month period ended September 30, 1995 as compared with the same period in 1994 reflects the acquisition of Hospital Supply Corporation of America, a hospital buying group and significant former customer of NDM, by Columbia Healthcare System, which is not a customer of NDM. This acquisition took place mid year 1994 and the revenues of the first six months of 1994 included revenues of the former customer. In addition, critical care product revenue was lower than in the first nine months of 1994 as a result of the introduction of a new line of products during 1994 which initially experienced transition difficulties during the third quarter of 1994. NDM believes it has resolved the issues associated with this product and that market acceptance has improved and sales stabilized. However, revenues for the product are at a lower level than in the first six months of 1994 which was prior to the introduction. Critical care product revenues during the third quarter showed an increase over the third quarter 1994 due to the effect of product backorders incurred during the third quarter of 1994 caused by two key suppliers moving their manufacturing operations. An inventory reduction program implemented in the third quarter of 1994 by NDM's primary distributor impacted both patient care and critical care products accounting for a substantial portion of the increase in the third quarter of 1995 from the third quarter of 1994. Cost of sales decreased 4.6% and 6.8% from comparable three and nine month periods ended September 30, 1995. The decrease was primarily due to the following: 1) The third quarter of 1994 cost of sales was increased by the write off of $603,000 in excess and obsolete inventory due to new foot pump product introductions and the establishment of an accrual for anticipated rework/warranty costs related to critical care products of $192,000 and 2) the third quarter of 1995 cost of sales was reduced by $135,000 due to the settlement of certain provisions in a distributor contract. The reduction in cost of sales for the nine month period ended September 30, 1995 compared with the same period in 1994 reflects the decrease in revenues for the same periods combined with the third quarter 1995 activity discussed above. Operating expenses, consisting of research and development, sales and marketing, distribution, general and administrative, royalty and amortization expenses, decreased 35.7% and 25.1% in the three and nine month periods ended September 30, 1995 from the same periods in 1994. The decrease in operating expenses was primarily due to the following: 1) The third quarter of 1994 general and administrative expenses included an accrual for anticipated legal costs associated with patent defense of $300,000, an additional provision for potentially uncollectable accounts of $500,000 and restructuring expenses of $756,000 related to various severance and outplacement costs and 2) the third quarter of 1995 operating expenses were reduced due to cost savings in the sales and marketing expenses by approximately $500,000 including an $80,000 reduction to accrued incentive compensation; cost reductions in research and development expense of approximately $150,000 offset by an accrual in general and administrative costs for professional fees incurred related to the sale of substantially all the assets of the company of approximately $300,000 as well as an increase in the provision for doubtful accounts of $45,000. The reduction in operating expenses for the nine month period ended September 30, 1995 compared with the same period in 1994 includes a decrease in distribution expenses of $560,000 as a result of the reduced revenues and a revision to a contract with the Company's primary distributor, the factors impacting the third quarter and cost reductions implemented during the third quarter of 1994 as well as continued cost containment during 1995. Net interest expense increased by 18.9% in the third quarter and by 29.4% in the nine months ended September 30, 1995 when compared to the same period in 1994. This resulted from additional borrowings under the line of credit of $1,200,000 during the third quarter combined with increased interest rates on the borrowing facilities. Other income (expense) consists primarily of royalty income offset by other expenses such as certain bank fees and other non operating expenses. The higher income relates to increased royalty income for the nine month period during 1995 of $160,000. The expense of $178,000 incurred during the nine month period ended September 30, 1994 represented non-recurring costs associated with financial activities due to the restructuring of the company, and the write off of certain equipment. The provision for income taxes includes franchise taxes and federal income tax. This primarily reflects the change in income before income taxes. Under "fresh start" accounting for financial reporting purposes in accordance with the American Institute of Certified Public Accountants Statements of Position 90-7 and current accounting for income tax rules, utilization of the NOL carryforwards are required to offset intangible assets and do not offset income tax expense. Therefore, a federal income tax provision has been appropriately recorded. Liquidity and Capital Resources NDM's net working capital of $4.4 million at September 30, 1995 increased $868,000 from the December 31, 1994 levels. Cash of $1,977,000 increased $847,000 from the December 31, 1994 level primarily due to the additional draw on the revolving line of credit of $1,200,000 offset by the payment of long-term debt. Receivables decreased $1,014,000 approximately 50% of which was due to the settlement of receivables related to a distribution contract collected in the third quarter as well as normal fluctuations from year end levels. The receivables from the Diversified Liquidating Trust decreased from December 31, 1994 level due to the collection of amounts due from the Trust under the Plan of Reorganization of MEI Diversified, Inc. Inventories increased $664,000 from the December 31, 1994 level the majority of which occurred in raw materials. Current liabilities decreased $863,000 from the December 31, 1994 level due primarily to a reduction in accounts payable and accrued liabilities of $2,062,000 offset by the additional borrowing under the line of credit facility of $1,200,000. As of September 30, 1995, NDM had an outstanding balance of $3,700,000 under its line of credit agreement. The line of credit facility has a maximum amount of $4,000,000 and the term is through June 30, 1997. The line of credit is secured by a first security interest in substantially all of NDM's assets. The interest rate on the line of credit is one half of one percent over the prime rate. NDM's credit facility also include a floating rate option note with an outstanding balance of $5.6 million at September 30, 1995, due in semi-annual installments of $400,00 which commenced on November 1, 1992 and matures May 1, 2002. The lender sets the interest rate on a weekly basis based on market conditions for similar debt. This rate was 6.28% at December 31, 1994 and 5.81% at September 30, 1995. The financial arrangements contain various covenants related to cash flow, debt to tangible net worth, current ratio and capital expenditures and the Company is in compliance with these covenants. In November 1995, the Company's lender agreed to increase the Company's lending facility by $1,000,000. The additional funds are to be provided through a six month demand note with an interest rate of one half of one percent over the prime rate with a one percent fee. The Company believes that the increase in the line of credit will provide the Company with sufficient cash to meet its obligations until closing of the CONMED transaction, provided that such closing occurs by January 31, 1996. If such closing is delayed or does not occur, the Company will likely need to raise additional capital to continue operations. There can be no assurance that the Company will be able to raise any additional capital or that the terms will be satisfactory the Company. On October 18, 1995, the Company and CONMED Corporation ("CONMED") entered into an Asset Purchase Agreement (the "Agreement"), pursuant to which CONMED will purchase substantially all of the Company's assets, except its hydrogel wound care business outside of the United States, Mexico and Canada and its foot pump business. CONMED will assume liabilities related to the assets being acquired. The purchase price for the assets is $32,134,299, subject to certain adjustments for the disposition of the excluded assets and satisfaction of liabilities related to the excluded assets. In addition, the purchase price will be adjusted if the Company's net assets, subject to certain adjustments for excluded assets and liabilities and depreciation and amortization, increase by more than $1,700,000 or decrease by more than $1,000,000 from August 31, 1995 through closing. CONMED is also obligated to enter into certain agreements with the purchaser of the Company's international wound care business. The consummation of the Agreement is subject to additional conditions including the approval of the shareholders of the Company and required regulatory approvals. Additionally, pursuant to a separate letter of intent agreement between the Company and a third party, the Company will sell the assets and technology of the international wound care business to the third party and is in the process of negotiating a definitive agreement. Following consummation of the above transactions, the Company intends to wind-down operations and liquidate its remaining assets. Additionally, the Company intends to distribute the net proceeds from the above discussed asset sales to its shareholders. The proposed CONMED transaction is subject to regulatory approvals and approval by the Company's shareholders. The Company has not recorded any adjustments to the carrying amounts of its assets and liabilities to adopt the liquidation basis of accounting or the contingencies that may be triggered by these transactions, such as the repayment of outstanding debt and severance liabilities. Under the liquidation basis of accounting, assets would be adjusted to their estimated realizable value and liabilities would be adjusted to their estimated settlement amount. As of September 30, 1995, the Company did not have any material commitments for capital expenditures. PART II. OTHER INFORMATION Item 3. Legal Proceedings NovaMedix, Limited Following is an update to the previously disclosed action entitled NovaMedix Limited vs. NDM (U.K). In July, 1995, a U.K. patent court ruled in favor of NovaMedix Limited in a patent infringement suit against NDM (U.K). the distributor of NDM's product in the U.K. This ruling has effectively impaired the Company's ability to market its foot pump compression products in the United Kingdom. NDM (U.K.) is still evaluating whether it will pursue its right to appeal the decision. Additionally, following the ruling, NovaMedix has appealed to the court to recover its costs and damages from NDM even though NDM was not a party to the action. The Company's patent counsel has been informed that the plaintiff's litigation costs may approximate $500,000. No provision has been made in the accompanying consolidated financial statements to cover plaintiff litigation costs. The Company has already applied to the court to set aside NovaMedix's application to recover its costs from NDM. Item 5. Other Information On October 18, 1995, the Company and CONMED Corporation ("CONMED") entered into an Asset Purchase Agreement (the "Agreement"), pursuant to which CONMED will purchase substantially all of the Company's assets, except its hydrogel wound care business outside of the United States, Mexico and Canada and its foot pump business. CONMED will assume liabilities related to the assets being acquired. The purchase price for the assets is $32,134,299, subject to certain adjustments for the disposition of the excluded assets and satisfaction of liabilities related to the excluded assets. In addition, the purchase price will be adjusted if the Company's net assets, subject to certain adjustments for excluded assets and liabilities and depreciation and amortization, increase by more than $1,700,000 or decrease by more than $1,000,000 from August 31, 1995 through closing. CONMED is also obligated to enter into certain agreements with the purchaser of the Company's international wound care business. The consummation of the Agreement is subject to additional conditions including the approval of the shareholders of the Company and required regulatory approvals. Additionally, pursuant to a separate letter of intent agreement between the Company and a third party, the Company will sell the assets and technology of the international wound care business to the third party and is in the process of negotiating a definitive agreement. Following consummation of the above transactions, the Company intends to wind-down operations and liquidate its remaining assets. Additionally, the Company intends to distribute the net proceeds from the above discussed asset sales to its shareholders. The proposed CONMED transaction is subject to regulatory approvals and approval by the Company's shareholders. The Company has not recorded any adjustments to the carrying amounts of its assets and liabilities to adopt the liquidation basis of accounting or the contingencies that may be triggered by these transactions, such as the repayment of outstanding debt and severance liabilities. Under the liquidation basis of accounting, assets would be adjusted to their estimated realizable value and liabilities would be adjusted to their estimated settlement amount. SIGNATURES Pursuant to the requirements of the Securities Exchange Act of 1934, Registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized. NEW DIMENSIONS IN MEDICINE, INC. Date: November 13, 1995 By /s/ William F. Shea ------------------------------------ William F. Shea Chief Executive Officer (Principal Executive Officer) Date: November 13, 1995 By /s/ Philip J. Oliver ------------------------------------ Philip J. Oliver Vice President of Finance (Principal Accounting and Financial Officer)