Oculogica, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oculogica, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EyeBOX SNAP, EyeBOX EBX-4.1, EyeBOX (Model EBX-4)
6
Total
5
Cleared
1
Denied
Oculogica, Inc. has 5 FDA 510(k) cleared medical devices. Based in New York, US.
Latest FDA clearance: Jun 2026. 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.
Regulatory submissions have been managed by Hogan Lovells US LLP and Hogan Lovells.
FDA 510(k) Regulatory Record - Oculogica, Inc.
6 devices