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.
510(k) submissions have been managed by The OrthoMedix Group, Inc. as regulatory consultant.
4 devices