Customsurg AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Customsurg AG - FDA 510(k) Cleared Devices
Recent clearances: CustomSurg OrthoPlanner
1
Total
1
Cleared
0
Denied
Customsurg AG has 1 FDA 510(k) cleared medical devices. Based in Zurich, CH.
Latest FDA clearance: Jul 2025. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Customsurg AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Customsurg AG
1 devices