FDA applicant
Wright Medical Technology, Inc. (Stryker)
FDA records 5 decisions for Wright Medical Technology, Inc. (Stryker) (Memphis, TN) from 2024 to 2026: 5 510(k) clearances. Most are in product codes HSN (Prosthesis, Ankle, Semi-Constrained, Cemented…) and HTN (Washer, Bolt Nut). Since 2016 its 510(k)s took a median of 134 days from receipt to decision, against 67 for FDA’s reviews in the same codes and years. Its devices cite 10 predicates, 2 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Wright Medical Technology, Inc. (Stryker Corporation)”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Wright Medical Technology, Inc. (Stryker)’s devices, and how often a recall has named them.
FDA decisions per year
3in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2024.
Planning a device like Wright Medical Technology, Inc.…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Wright”
FDA records each applicant name separately; these may or may not be the same firm.