Ophtecs Corporation - FDA 510(k) Cleared Devices

Ophtecs Corporation has 1 FDA 510(k) cleared medical devices. Based in Kobe, JP.

Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Ophtecs Corporation Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Andre Vision and Device Research as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.