Medicrea International S.A.S. (Medtronic) 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. (Medtronic) - FDA 510(k) Cleared Devices
Recent clearances: UNiD™ Spine Analyzer (SW3002), IB3D™ PL Spinal System (A24000000 / IB3D Universal Implant Inserter), UNiD™ Spine Analyzer
4
Total
4
Cleared
0
Denied
Medicrea International S.A.S. (Medtronic) has 4 FDA 510(k) cleared medical devices. Based in Rillieux-La-Pape, FR.
Latest FDA clearance: May 2026. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Medicrea International S.A.S. (Medtronic) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medicrea International S.A.S. (Medtronic)
4 devices