W&H Dentalwerk Buermoss GmbH
AustriaFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Proxeo ULTRA (PB-510, PB-520 and PB-530) Ref K223173
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does W&H Dentalwerk Buermoss GmbH have in the registry?
The registry currently lists 2 devices for W&H Dentalwerk Buermoss GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list W&H Dentalwerk Buermoss GmbH's devices?
Among its 2 most recently registered devices, W&H Dentalwerk Buermoss GmbH has devices listed in FDA 510(k) (2 devices).
What risk classes do W&H Dentalwerk Buermoss GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for W&H Dentalwerk Buermoss GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from W&H Dentalwerk Buermoss GmbH in the registry?
The most recently registered devices listed for W&H Dentalwerk Buermoss GmbH include AMADEO, M-UK1015 (incl. attachments and accessories) and Proxeo ULTRA (PB-510, PB-520 and PB-530).