Collafirm, LLC
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Bovine Pericardium Patch Ref K141721
Regimes: 510(k) Registry: 510(k)Fibrillar Collagen Wound Dressing Ref K120250
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Collafirm, LLC have in the registry?
The registry currently lists 2 devices for Collafirm, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Collafirm, LLC's devices?
Among its 2 most recently registered devices, Collafirm, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Collafirm, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Collafirm, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Collafirm, LLC in the registry?
The most recently registered devices listed for Collafirm, LLC include BOVINE PERICARDIUM PATCH and FIBRILLAR COLLAGEN WOUND DRESSING.