Companion Spine France is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Companion Spine France - FDA 510(k) Cleared Devices
Recent clearances: Companion Spine DIAM™ Instrumentation
1
Total
1
Cleared
0
Denied
Companion Spine France has 1 FDA 510(k) cleared medical devices. Based in M?rignac, FR.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Companion Spine France Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Companion Spine France
1 devices