Oco Biomedical
United Statesfrom the FDA registration address FDA FEI 1627417
Oco Biomedical is a medical device manufacturer, with 750 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 12 Nov 2026.
- Devices
- 750
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 746
- FDA 510(k) 4
- Device classes
- FDA Class II 422
- FDA Class I 328
- Identifiers
- FDA FEI 1627417
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 750 devicesShowing 1-50 of 750
Company details
- FDA FEI number
- 1627417
- Address
- 9550 San Mateo Blvd NE Ste C, ALBUQUERQUE, NM, 87113
Frequently asked questions
How many devices does Oco Biomedical have in the registry?
The registry currently lists 750 devices for Oco Biomedical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oco Biomedical's devices?
Among its 50 most recently registered devices, Oco Biomedical has devices listed in FDA GUDID (50 devices).
What risk classes do Oco Biomedical's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Oco Biomedical's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oco Biomedical in the registry?
The most recently registered devices listed for Oco Biomedical include 10 PACK OT EQUATOR HOUSING CAP WITH BLACK INSERT OT CAP 10, 4 PACK OT EQUATOR HOUSING CAP WITH BLACK INSERT OT CAP 4, 4 PACK OT EQUATOR PINK INSERTS OT PINK 4 and 2 PACK OT EQUATOR IMPRESSION COPING OT PU 2.