Kinetix Instruments
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Endoscopic Carpal Tunnel Release System Ref K933470
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kinetix Instruments have in the registry?
The registry currently lists 1 device for Kinetix Instruments. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kinetix Instruments's devices?
Among its 1 most recently registered device, Kinetix Instruments has devices listed in FDA 510(k) (1 device).
What risk classes do Kinetix Instruments's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kinetix Instruments's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kinetix Instruments in the registry?
The most recently registered devices listed for Kinetix Instruments include ENDOSCOPIC CARPAL TUNNEL RELEASE SYSTEM.