Centrix, Inc.

Centrix, Inc. — FDA 510(k) Submissions

Centrix, Inc. has submitted 47 FDA 510(k) premarket notifications since 1979, of which 47 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Cement, Dental, Agent, Tooth Bonding, Resin, Material, Tooth Shade, Resin, Varnish, Cavity, Burnisher, Operative . Use the specialty filter in the sidebar to narrow results.