Implanet is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Implanet - FDA 510(k) Cleared Devices
Recent clearances: SWINGO-3D Lumbar Cage System, JAZZ Spinal System, JAZZ Spinal System
3
Total
3
Cleared
0
Denied
Implanet has 3 FDA 510(k) cleared medical devices. Based in Allee Francois Magendie, FR.
Latest FDA clearance: Feb 2026. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Implanet Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by MRC Global, LLC and MRC Global.
FDA 510(k) Regulatory Record - Implanet
3 devices