Kavo America Corporation

Kavo America Corporation — FDA 510(k) Submissions

Kavo America Corporation has submitted 4 FDA 510(k) premarket notifications since 2003, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Powder, Porcelain, Laser, Fluorescence Caries Detection, Airbrush, System, Image Processing, Radiological . Use the specialty filter in the sidebar to narrow results.