# Stryker Corporation (Tornier, Inc.)

- Location (FDA's records): Bloomington, MN
- FDA decisions: 5 (2024–2026): 5 510(k) clearances
- Names in FDA's records: Stryker Corporation (Tornier, Inc.) (3); Stryker Corporation (Tornier, S.A.S.) (2)
- Product codes: PHX (3), KWS (2)
- 510(k) review time since 2016: median 139 days, against 130 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 11 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Tornier, Inc.: 9 (https://510kreport.com/company/tornier)
- Akunah Pty, Ltd.: 1 (https://510kreport.com/company/akunah)

## Firms that cite its devices most
- Tornier, Inc.: 1 (https://510kreport.com/company/tornier)

## Its most-cited devices
- K241878: Tornier Humeral Reconstruction System (Tornier HRS); Tornier Perform Humeral System - Stem (Tornier PHS-Stem) (2024), cited by 1
- K241491: Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed Glenoid (2024), cited by 1

## Recent decisions
- K260102: Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System (Jun 12, 2026)
- K253674: Blueprint Patient-Specific Instrumentation (Apr 3, 2026)
- K241878: Tornier Humeral Reconstruction System (Tornier HRS); Tornier Perform Humeral System - Stem (Tornier PHS-Stem) (Dec 6, 2024)
- K241491: Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed Glenoid (Oct 10, 2024)
- K241609: Tornier Humeral Reconstruction System (Tornier HRS) (Sep 10, 2024)

Source page: https://510kreport.com/company/stryker-tornier