Tornier, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tornier, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Tornier Perform Advanced Glenoid, Tornier Perform™ Reversed Monopost Glenoid (Perform Mono), Tornier Humeral Reconstruction System Max (Tornier HRS Max)
52
Total
52
Cleared
0
Denied
Tornier, Inc. has 52 FDA 510(k) cleared orthopedic devices. Based in Beverly, US.
Latest FDA clearance: Jul 2026. Active since 2000.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Tornier, Inc.
52 devices
Cleared
Jul 22, 2026
Tornier Perform Advanced Glenoid
Orthopedic
139d
Cleared
Jan 08, 2026
Tornier Perform™ Reversed Monopost Glenoid (Perform Mono)
Orthopedic
128d
Cleared
Oct 30, 2025
Tornier Humeral Reconstruction System Max (Tornier HRS Max)
Orthopedic
150d
Cleared
Oct 31, 2023
Tornier Humeral Nail and Tornier Long Humeral Nail
Orthopedic
264d
Cleared
Oct 14, 2022
Tornier Perform Humeral System – Fracture
Orthopedic
198d
Cleared
Sep 14, 2022
Tornier Perform Humeral System – Stemless
Orthopedic
212d
Cleared
Nov 12, 2021
Tornier Perform™ Patient-Matched Primary Reversed Glenoid and BLUEPRINT™...
Orthopedic
193d
Cleared
Oct 26, 2021
Tomier Perform™ Reversed Glenoid Cannulated Glenospheres
Orthopedic
29d
Cleared
Sep 11, 2020
PERFORM Humeral System – Stem
Orthopedic
116d
Cleared
Aug 05, 2020
LATITUDE EV™ Total Elbow Arthroplasty
Orthopedic
254d
Cleared
Jul 17, 2019
ORTHOLOC™ SPS Shoulder Plating System
Orthopedic
21d
Cleared
Jun 14, 2019
AEQUALIS FLEX REVIVE Shoulder System
Orthopedic
30d
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