This AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
This AG - FDA 510(k) Cleared Devices
Recent clearances: System Sophi
1
Total
1
Cleared
0
Denied
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.
FDA 510(k) Regulatory Record - This AG
1 devices