Oculogica, Inc. - FDA 510(k) Cleared Devices
5
Total
4
Cleared
1
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.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
5 devices