Spinevision, S.A.S. is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Spinevision, S.A.S. - FDA 510(k) Cleared Devices
Recent clearances: Hexanium PLIF, Hexanium ACIF, Hexanium TLIF
5
Total
5
Cleared
0
Denied
Spinevision, S.A.S. has 5 FDA 510(k) cleared medical devices. Based in Antony, FR.
Last cleared in 2022. Active since 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Spinevision, S.A.S. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Lince Consulting, LLC and Orgenix, LLC.
FDA 510(k) Regulatory Record - Spinevision, S.A.S.
5 devices