Surgentec is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgentec - FDA 510(k) Cleared Devices
Recent clearances: TiLink-L Joint Fusion System, 3D GraftRasp System, 3D GraftRasp System
3
Total
3
Cleared
0
Denied
Surgentec has 3 FDA 510(k) cleared medical devices. Based in Boca Raton, US.
Last cleared in 2023. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Surgentec Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Surgentec
3 devices