This AG - FDA 510(k) Cleared Devices

This AG has 1 FDA 510(k) cleared medical devices. Based in Heerbrugg, CH.

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

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

510(k) submissions have been managed by Regulatory Pathways Group, Inc. as regulatory consultant.