Biorec US, Inc.
Country not established
- Devices
- 1
What Biorec US, Inc. makes
Biorec Us, Inc. manufactures the BIOMATT-1, a medical device designed for wound care or tissue integration applications, likely intended for surgical or trauma settings.
The BIOMATT-1 is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Biomatt-1 Ref K841392
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biorec Us, Inc. have in the registry?
The registry currently lists 1 device for Biorec Us, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biorec Us, Inc.'s devices?
Among its 1 most recently registered device, Biorec Us, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Biorec Us, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Biorec Us, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biorec Us, Inc. in the registry?
The most recently registered devices listed for Biorec Us, Inc. include BIOMATT-1.