Medical Device Manufacturer · US , Walker , MI

Titmus Optical, Inc.

3 submissions · 3 cleared · Since 1983
3
Total
3
Cleared
0
Denied

Titmus Optical, Inc. — FDA 510(k) Submissions

Titmus Optical, Inc. has submitted 3 FDA 510(k) premarket notifications since 1983, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Photostimulator, Ac-powered, Lens, Spectacle, Non-custom (prescription), Tester, Color Vision . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
Filters
Filter by Specialty
All3 Ophthalmic 3