Biomup S.A.
FranceFDA applicant, unverified
- Devices
- 1
What Biomup S.A. makes
Biomup S.A. manufactures COVAMESH, a surgical mesh designed for hernia repair and related reconstructive procedures.
The company’s portfolio is regulated under FDA’s Class II device classification, with COVAMESH authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) registry. Biomup S.A. is based in the United States.
Catalogue
Covamesh Ref K130428
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biomup S.A. have in the registry?
The registry currently lists 1 device for Biomup S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biomup S.A.'s devices?
Among its 1 most recently registered device, Biomup S.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Biomup S.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Biomup S.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biomup S.A. in the registry?
The most recently registered devices listed for Biomup S.A. include COVAMESH.