Visioncare Devices, Inc.

Visioncare Devices, Inc. — FDA 510(k) Submissions

Visioncare Devices, Inc. has submitted 5 FDA 510(k) premarket notifications since 1991, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Instrument, Vitreous Aspiration And Cutting, Ac-powered, Unit, Phacofragmentation . Use the specialty filter in the sidebar to narrow results.