CAO Group, Inc.

CAO Group, Inc. — FDA 510(k) Submissions

CAO Group, Inc. has submitted 31 FDA 510(k) premarket notifications since 2001, of which 31 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Powered Laser Surgical Instrument, Agent, Tooth Bonding, Resin, Activator, Ultraviolet, For Polymerization, Varnish, Cavity, Massager, Vacuum, Radio Frequency Induced Heat . Use the specialty filter in the sidebar to narrow results.