Pixee Medical S.A.S. is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Pixee Medical S.A.S. - FDA 510(k) Cleared Devices
Recent clearances: Knee+
1
Total
1
Cleared
0
Denied
Pixee Medical S.A.S. has 1 FDA 510(k) cleared medical devices. Based in Besançon, FR.
Latest FDA clearance: Apr 2026. Active since 2026. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Pixee Medical S.A.S. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pixee Medical S.A.S.
1 devices