Duerr Dental AG

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.