Oculomotor Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oculomotor Technologies - FDA 510(k) Cleared Devices
Recent clearances: VERVE
1
Total
1
Cleared
0
Denied
Oculomotor Technologies has 1 FDA 510(k) cleared medical devices. Based in Princeton, US.
Latest FDA clearance: Jun 2024. Active since 2024. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Oculomotor Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by RQM+ as regulatory consultant.
FDA 510(k) Regulatory Record - Oculomotor Technologies
1 devices