Dentlight, Inc.

Dentlight, Inc. — FDA 510(k) Submissions

Dentlight, Inc. has submitted 4 FDA 510(k) premarket notifications since 2005, of which 4 received clearance as substantially equivalent to a predicate device.

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