Wintecare SA is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Wintecare SA - FDA 510(k) Cleared Devices
Recent clearances: T-PLUS
1
Total
1
Cleared
0
Denied
Wintecare SA has 1 FDA 510(k) cleared medical devices. Based in Chiasso, CH.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Wintecare SA Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Wintecare SA
1 devices