Addent, Inc.

Addent, Inc. — FDA 510(k) Submissions

Addent, Inc. has submitted 7 FDA 510(k) premarket notifications since 2005, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Light, Operating, Dental, Diagnostic Light, Soft Tissue Detector, Activator, Ultraviolet, For Polymerization, Caries Detector, Laser Light, Transmission, Composite Resin Warmer . Use the specialty filter in the sidebar to narrow results.