Biorest, Inc.
Country not established
- Devices
- 1
What Biorest, Inc. makes
Biorest, Inc. manufactures the BR-2 BIOREST, a medical device designed for tissue regeneration or wound care applications, likely intended for surgical or dermatological use.
The BR-2 BIOREST is classified as a Class II device under FDA regulations and is authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Br-2 Biorest Ref K873920
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biorest, Inc. have in the registry?
The registry currently lists 1 device for Biorest, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biorest, Inc.'s devices?
Among its 1 most recently registered device, Biorest, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Biorest, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Biorest, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biorest, Inc. in the registry?
The most recently registered devices listed for Biorest, Inc. include BR-2 BIOREST.