Ortho-Med, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3019455
- Devices
- 2,897
- Registrations
- FDA
- FDA recalls
- 0
What Ortho-Med, Inc. makes
Ortho-Med, Inc. manufactures reusable surgical instruments for orthopaedic and spinal procedures, including bone curettes, spinal rongeurs, general-purpose surgical scissors, orthopaedic bone pins, bone holding forceps, dressing forceps, osteotomes, and suturing needle holders.
The company’s products are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Catalogue
Search and filter all 2,897 devicesShowing 1-50 of 2,897
Company details
- FDA FEI number
- 3019455
- Address
- 14875 SW 72nd Ave, Tigard, OR, 97224
Frequently asked questions
How many devices does ORTHO-MED, INC. have in the registry?
The registry currently lists 2897 devices for ORTHO-MED, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ORTHO-MED, INC.'s devices?
Among its 50 most recently registered devices, ORTHO-MED, INC. has devices listed in FDA GUDID (50 devices).
What risk classes do ORTHO-MED, INC.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for ORTHO-MED, INC.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from ORTHO-MED, INC. in the registry?
The most recently registered devices listed for ORTHO-MED, INC. include ORTHOMED OM 90-1865, ORTHOMED OM 59-0362, ORTHOMED OM 59-0363 and ORTHOMED OM 2010.