Hennert S.A.
FranceFDA applicant, unverified
- Devices
- 1
What Hennert S.A. makes
Hennert S.A. manufactures a Class I medical device identified as HENNERT SA.
The device is regulated under U.S. FDA 510(k) requirements and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Hennert SA Ref K952734
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hennert S.A. have in the registry?
The registry currently lists 1 device for Hennert S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hennert S.A.'s devices?
Among its 1 most recently registered device, Hennert S.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Hennert S.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hennert S.A.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Hennert S.A. in the registry?
The most recently registered devices listed for Hennert S.A. include HENNERT SA.