Ocular Instruments, Inc.

Ocular Instruments, Inc. — FDA 510(k) Submissions

Ocular Instruments, Inc. has submitted 50 FDA 510(k) premarket notifications since 1984, of which 50 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Lens, Contact, Polymethylmethacrylate, Diagnostic, Prism, Gonioscopic, Lens, Surgical, Laser, Accesssory, Ophthalmic Laser, Ring, Ophthalmic (flieringa), Keratoprosthesis, Temporary Implant, Surgical Use . Use the specialty filter in the sidebar to narrow results.