Medical Device Manufacturer · DE , Wetzlar

Oculus Optikger?te GmbH

2 submissions · 2 cleared · Since 2021
2
Total
2
Cleared
0
Denied

Oculus Optikger?te GmbH — FDA 510(k) Submissions

Oculus Optikger?te GmbH has submitted 2 FDA 510(k) premarket notifications since 2021, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device, Analysis, Anterior Segment . Use the specialty filter in the sidebar to narrow results.

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