Scandiags AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Scandiags AG - FDA 510(k) Cleared Devices
Recent clearances: ScanDiags Ortho L-Spine MR-Q
1
Total
1
Cleared
0
Denied
Scandiags AG has 1 FDA 510(k) cleared medical devices. Based in Wallisellen, CH.
Latest FDA clearance: Feb 2025. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Scandiags AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Scandiags AG
1 devices