Medical Device Manufacturer · US , Laguna Beach , CA

Od-Os GmbH

4 submissions · 4 cleared · Since 2009
4
Total
4
Cleared
0
Denied

Od-Os GmbH — FDA 510(k) Submissions

Od-Os GmbH has submitted 4 FDA 510(k) premarket notifications since 2009, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laser, Ophthalmic, Powered Laser Surgical Instrument . Use the specialty filter in the sidebar to narrow results.

4 devices
1–4 of 4
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All4 Ophthalmic 2 General & Plastic Surgery 2