Medicrea International S.A.S is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Medicrea International S.A.S - FDA 510(k) Cleared Devices
Recent clearances: LigaPASS™ System
1
Total
1
Cleared
0
Denied
Medicrea International S.A.S has 1 FDA 510(k) cleared medical devices. Based in Rillieux-La-Pape, FR.
Latest FDA clearance: May 2026. Active since 2026. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Medicrea International S.A.S Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medicrea International S.A.S
1 devices