Medical Device Manufacturer · US , New York , NY

Oculogica, Inc. - FDA 510(k) Cleared Devices

5 submissions · 4 cleared · Since 2018

Total

Cleared

Denied

Oculogica, Inc. has 4 FDA 510(k) cleared medical devices. Based in New York, US.

Latest FDA clearance: Apr 2025. Active since 2018. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Oculogica, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Oculogica, Inc.

5 devices

1-5 of 5