Coligne AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Coligne AG - FDA 510(k) Cleared Devices
Recent clearances: GII Spinal Fixation System, ostaPek Interbody Fusion Cages, Trabis
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.
FDA 510(k) Regulatory Record - Coligne AG
4 devices