Bionexus, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Femtest Ref K844173
Regimes: 510(k) Registry: 510(k)Nexadent (Dental Cement) Ref K870209
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bionexus, Inc. have in the registry?
The registry currently lists 2 devices for Bionexus, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bionexus, Inc.'s devices?
Among its 2 most recently registered devices, Bionexus, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Bionexus, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Bionexus, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bionexus, Inc. in the registry?
The most recently registered devices listed for Bionexus, Inc. include FEMTEST and NEXADENT (DENTAL CEMENT).