Tearscience, Inc.

Tearscience, Inc. — FDA 510(k) Submissions

Tearscience, Inc. has submitted 9 FDA 510(k) premarket notifications since 2009, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Eyelid Thermal Pulsation System, Camera, Ophthalmic, Ac-powered . Use the specialty filter in the sidebar to narrow results.