Amann Girrbach America, Inc.
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ceramill Zi Ref K063511
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Amann Girrbach America, Inc. have in the registry?
The registry currently lists 1 device for Amann Girrbach America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amann Girrbach America, Inc.'s devices?
Among its 1 most recently registered device, Amann Girrbach America, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Amann Girrbach America, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Amann Girrbach America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Amann Girrbach America, Inc. in the registry?
The most recently registered devices listed for Amann Girrbach America, Inc. include CERAMILL ZI.