Coligne AG - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Coligne AG has 4 FDA 510(k) cleared medical devices. Based in Zurich, CH.
Last cleared in 2021. Active since 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Coligne AG Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Coligne AG
4 devices