WAVE Medical AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
WAVE Medical AG - FDA 510(k) Cleared Devices
Recent clearances: WAVE PTA Balloon Catheter
1
Total
1
Cleared
0
Denied
WAVE Medical AG has 1 FDA 510(k) cleared medical devices. Based in Neuhausen Am Rheinfall, CH.
Latest FDA clearance: May 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by WAVE Medical AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - WAVE Medical AG
1 devices