Stephanix is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Stephanix - FDA 510(k) Cleared Devices
Recent clearances: D²RS and D²RS 9090, D²RS and D²RS 9090, MOVIX DReamy
3
Total
3
Cleared
0
Denied
Stephanix has 3 FDA 510(k) cleared medical devices. Based in La Ricamarie, FR.
Last cleared in 2022. Active since 2021. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Stephanix Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kamm & Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Stephanix
3 devices