Sunstar Suisse S.A. is one of 139 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Sunstar Suisse S.A. - FDA 510(k) Cleared Devices
Recent clearances: GrindCare System
1
Total
1
Cleared
0
Denied
Sunstar Suisse S.A. has 1 FDA 510(k) cleared medical devices. Based in Etoy, CH.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Sunstar Suisse S.A. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Biologics Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Sunstar Suisse S.A.
1 devices