Medacta International, SA is one of 130 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Medacta International, SA - FDA 510(k) Cleared Devices
Recent clearances: GMK Extension, MSS - Humeral reverse liners extension
2
Total
2
Cleared
0
Denied
Medacta International, SA has 2 FDA 510(k) cleared medical devices. Based in Castel San Pietro, CH.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Medacta International, SA Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medacta USA as regulatory consultant.
FDA 510(k) Regulatory Record - Medacta International, SA
2 devices