Johnson & Johnson Surgical Vision, Inc.

Johnson & Johnson Surgical Vision, Inc. — FDA 510(k) Submissions

Johnson & Johnson Surgical Vision, Inc. has submitted 4 FDA 510(k) premarket notifications since 2019, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Unit, Phacofragmentation, Folders And Injectors, Intraocular Lens (iol), Ophthalmic Femtosecond Laser . Use the specialty filter in the sidebar to narrow results.