Medical Device Manufacturer · DE , Bietigheim-Bissingen

Duerr Dental AG

3 submissions · 3 cleared · Since 2016
3
Total
3
Cleared
0
Denied

Duerr Dental AG — FDA 510(k) Submissions

Duerr Dental AG has submitted 3 FDA 510(k) premarket notifications since 2016, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Image Processing, Radiological, System, X-ray, Extraoral Source, Digital, Caries Detector, Laser Light, Transmission . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
Filters