Ets Gouverneur-Audigier
FranceFDA 510(k) applicant, unverified
- Devices
- 1
What Ets Gouverneur-Audigier makes
Ets Gouverneur-Audigier manufactures the Gouverneur-Audigier, a medical device designed for use in orthopedic surgery, specifically as a bone graft substitute or spacer in joint replacement procedures.
The device is classified as Class I under FDA regulations and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Gouverneur Audigier Ref K952758
510(k) 510(k)
Frequently asked questions
How many devices does Ets Gouverneur-Audigier have in the registry?
The registry currently lists 1 device for Ets Gouverneur-Audigier. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ets Gouverneur-Audigier's devices?
Among its 1 most recently registered device, Ets Gouverneur-Audigier has devices listed in FDA 510(k) (1 device).
What risk classes do Ets Gouverneur-Audigier's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ets Gouverneur-Audigier's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ets Gouverneur-Audigier in the registry?
The most recently registered devices listed for Ets Gouverneur-Audigier include GOUVERNEUR AUDIGIER.