Kerr Corporation

Kerr Corporation — FDA 510(k) Submissions

Kerr Corporation has submitted 32 FDA 510(k) premarket notifications since 2006, of which 32 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Material, Tooth Shade, Resin, Cord, Retraction, Activator, Ultraviolet, For Polymerization, Agent, Tooth Bonding, Resin, Cement, Dental . Use the specialty filter in the sidebar to narrow results.