Biomed Ent, Inc.
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Epi-Stop Nasal Gel/epistaxis pack Ref K230142
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biomed Ent, Inc. have in the registry?
The registry currently lists 1 device for Biomed Ent, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biomed Ent, Inc.'s devices?
Among its 1 most recently registered device, Biomed Ent, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Biomed Ent, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Biomed Ent, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Biomed Ent, Inc. in the registry?
The most recently registered devices listed for Biomed Ent, Inc. include Epi-Stop Nasal Gel/epistaxis pack.