Tornier S.A.S. - FDA 510(k) Cleared Devices
20
Total
19
Cleared
1
Denied
Tornier S.A.S. has 19 FDA 510(k) cleared medical devices. Based in Bloomington, US.
Latest FDA clearance: Feb 2024. Active since 2013.
Browse the FDA 510(k) cleared devices submitted by Tornier S.A.S. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Tornier S.A.S.
4 devices
Cleared
Feb 21, 2024
BLUEPRINT™ Patient Specific Instrumentation
Orthopedic
205d
Cleared
Jan 20, 2023
Blueprint Mixed Reality system
Orthopedic
154d
Not Cleared
Dec 16, 2022
Tornier Pyrocarbon Humeral Head
Orthopedic
311d
Cleared
Apr 15, 2021
BLUEPRINT™ Patient Specific Instrumentation
Orthopedic
156d