Stryker Corporation (Tornier, Inc.)

FDA Regulatory Profile

Stryker Corporation (Tornier, Inc.) appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 12, 2026.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K260102Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder SystemJune 12, 2026
K241878Tornier Humeral Reconstruction System (Tornier HRS); Tornier Perform Humeral System - Stem (Tornier December 6, 2024
K241609Tornier Humeral Reconstruction System (Tornier HRS)September 10, 2024