Newclip Technics - FDA 510(k) Cleared Devices
31
Total
31
Cleared
0
Denied
Newclip Technics has 31 FDA 510(k) cleared orthopedic devices. Based in Haute-Goulaine, FR.
Latest FDA clearance: Mar 2026. Active since 2006.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Newclip Technics
31 devices
Cleared
Mar 11, 2026
Xpert Hand
Orthopedic
96d
Cleared
Oct 01, 2025
Newclip Patient-matched instrumentation non sterile PSI
Orthopedic
202d
Cleared
Apr 23, 2025
Xpert Knee
Orthopedic
92d
Cleared
Feb 13, 2025
Newclip Patient-matched instrumentation non sterile PSI
Orthopedic
56d
Cleared
Nov 07, 2024
Newclip Patient-matched instrumentation non sterile PSI
Orthopedic
269d
Cleared
Jul 30, 2024
Activmotion S
Orthopedic
60d
Cleared
Oct 25, 2023
Newclip Patient-matched instrumentation non sterile PSI
Orthopedic
509d
Cleared
Jul 01, 2022
Footmotion Plating System
Orthopedic
49d
Cleared
Dec 16, 2021
Activmotion S DTO
Orthopedic
449d
Cleared
Nov 24, 2021
Xpert Wrist
Orthopedic
56d
Cleared
Nov 17, 2020
Activ Fuse
Orthopedic
95d
Cleared
Mar 02, 2018
Footmotion HammerToe
Orthopedic
197d