Mectron S.P.A.

Mectron S.P.A. — FDA 510(k) Submissions

Mectron S.P.A. has submitted 13 FDA 510(k) premarket notifications since 2009, of which 13 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Drill, Bone, Powered, Scaler, Ultrasonic, Instrument, Surgical, Sonic And Accessory/attachment, Airbrush, Activator, Ultraviolet, For Polymerization . Use the specialty filter in the sidebar to narrow results.