Cogent Light Technologies, Inc.

Cogent Light Technologies, Inc. — FDA 510(k) Submissions

Cogent Light Technologies, Inc. has submitted 5 FDA 510(k) premarket notifications since 1994, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Image, Illumination, Fiberoptic, For Endoscope, Light Source, Endoscope, Xenon Arc, Light, Surgical, Fiberoptic . Use the specialty filter in the sidebar to narrow results.