# Wright Medical Technology, Inc. (Stryker)

- Location (FDA's records): Memphis, TN
- FDA decisions: 5 (2024–2026): 5 510(k) clearances
- Names in FDA's records: Wright Medical Technology, Inc. (Stryker) (3); Wright Medical Technology, Inc. (Stryker Corporation) (2)
- Product codes: HSN (3), HTN (1), MQV (1)
- 510(k) review time since 2016: median 134 days, against 67 for FDA's reviews in the same codes and years (0 of 4 faster)
- Predicates its devices cite: 10 (2 its own); citations of its devices by later devices: 2 (2 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
- Wrightmedicaltechnologyinc: 8 (https://510kreport.com/company/wrightmedicaltechnologyinc)

## Its most-cited devices
- K250037: Incompass Total Ankle System (2025), cited by 1
- K241999: Prophecy Surgical Planning System (2024), cited by 1

## Recent decisions
- K253159: Prophecy Incompass Surgical Planning System (Jun 16, 2026)
- K251643: Synchfix EVT (Oct 29, 2025)
- K252085: Allomatrix (Allomatrix Injectable Putty; Allomatrix C; Allomatrix DR; Allomatrix Custom) (Sep 30, 2025)
- K250037: Incompass Total Ankle System (Jun 20, 2025)
- K241999: Prophecy Surgical Planning System (Nov 1, 2024)

Source page: https://510kreport.com/company/wright-medical-technology-stryker