Axia Orthopedics
United Statesfrom the FDA registration address FDA establishment FEI 3042953190
- Devices
- 8
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3042953190
- Address
- 2505 Se 11th Ave Ste 245, Portland, OR, 97202
Frequently asked questions
How many devices does AXIA ORTHOPEDICS have in the registry?
The registry currently lists 8 devices for AXIA ORTHOPEDICS. Devices recorded under merged duplicate company entries are counted once.
Which registries list AXIA ORTHOPEDICS's devices?
Among its 8 most recently registered devices, AXIA ORTHOPEDICS has devices listed in FDA GUDID (8 devices).
What risk classes do AXIA ORTHOPEDICS's devices fall under?
Among its 8 most recently registered devices, the classes recorded for AXIA ORTHOPEDICS's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from AXIA ORTHOPEDICS in the registry?
The most recently registered devices listed for AXIA ORTHOPEDICS include SOLOFIX Provisional Fixation System 500-101, SOLOFIX Provisional Fixation System 500-102, SOLOFIX Provisional Fixation System 500-105 and SOLOFIX Provisional Fixation System 500-103.