Apixia Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3008361230
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Apixia Digirex Digital Dental Rediography System Ref K120106
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3008361230
- Address
- 18688 E. SAN JOSE AVE, City of Industry, CA, 91748
Frequently asked questions
How many devices does APIXIA INC. have in the registry?
The registry currently lists 1 device for APIXIA INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list APIXIA INC.'s devices?
Among its 1 most recently registered device, APIXIA INC. has devices listed in FDA 510(k) (1 device).
What risk classes do APIXIA INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for APIXIA INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from APIXIA INC. in the registry?
The most recently registered devices listed for APIXIA INC. include APIXIA DIGIREX DIGITAL DENTAL REDIOGRAPHY SYSTEM.