# Wright Medical Corp.

- Location (FDA's records): Memphis, TN
- FDA decisions: 6 (1989–2021): 6 510(k) clearances
- Names in FDA's records: Wright Medical Corp. (3); Wright Medical (3)
- Product codes: DPW (1), HWC (1), JDR (1), KYF (1), KTT (1), HGM (1)
- 510(k) review time since 2016: median 190 days, against 84 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 7 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Wrightmedicaltechnologyinc: 2 (https://510kreport.com/company/wrightmedicaltechnologyinc)
- R&R Medical Corporation, Ltd.: 2 (https://510kreport.com/company/r-r-medical)
- Solana Surgical, LLC: 1 (https://510kreport.com/company/solana-surgical)

## Firms that cite its devices most
- New World Medical, Inc.: 2 (https://510kreport.com/company/new-world-medical)
- Life Spine, Inc.: 1 (https://510kreport.com/company/life-spine)
- Optonol, Ltd.: 1 (https://510kreport.com/company/optonol)
- Treace Medical Concepts, Inc.: 1 (https://510kreport.com/company/treace-medical-concepts)
- Wrightmedicaltechnologyinc: 1 (https://510kreport.com/company/wrightmedicaltechnologyinc)
- Trax Surgical: 1 (https://510kreport.com/company/trax-surgical)

## Its most-cited devices
- K905129: Baerveldt Glaucoma Implant (1991), cited by 3
- K203832: FuseForce™ Flex Dynamic Compression System (2021), cited by 2
- K162033: SALVATION External Fixation System (2017), cited by 2

## Recent decisions
- K203228: DART-FIRE EDGE Cannulated Screw System (May 11, 2021)
- K203832: FuseForce™ Flex Dynamic Compression System (May 7, 2021)
- K162033: SALVATION External Fixation System (Mar 6, 2017)
- K905129: Baerveldt Glaucoma Implant (Feb 11, 1991)
- K901015: Wright Pocket Dopplers Vascular & Obstetric (Nov 5, 1990)
- K892501: Wright Medical Fetasafe (Sep 12, 1989)

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