Medical Device Manufacturer · CH , Oensingen

Enbio Group AG

3 submissions · 3 cleared · Since 2021
3
Total
3
Cleared
0
Denied

Enbio Group AG — FDA 510(k) Submissions

Enbio Group AG has submitted 3 FDA 510(k) premarket notifications since 2021, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Sterilizer, Steam . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
Filters
All3 General Hospital 3