Genostis AF
SwitzerlandFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Genostis Osteosynthesis System Ref K242988
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Genostis AF have in the registry?
The registry currently lists 1 device for Genostis AF. Devices recorded under merged duplicate company entries are counted once.
Which registries list Genostis AF's devices?
Among its 1 most recently registered device, Genostis AF has devices listed in FDA 510(k) (1 device).
What risk classes do Genostis AF's devices fall under?
Among its 1 most recently registered device, the classes recorded for Genostis AF's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Genostis AF in the registry?
The most recently registered devices listed for Genostis AF include Genostis Osteosynthesis System.