Oculomotor Technologies - FDA 510(k) Cleared Devices

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.