510(k) Report

FDA applicant

Thackray USA

Ringoes, NJ5 decisions1986–19880 recalls

FDA records 5 decisions for Thackray USA (Ringoes, NJ) from 1986 to 1988: 5 510(k) clearances. Most are in product codes JDI (Prosthesis, Hip, Semi-Constrained…) and JDQ (Cerclage, Fixation). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Thackray USA’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Thackray USA since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Thackray USA by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • JDIProsthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2decisions
  • JDQCerclage, Fixation1decision
  • JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1decision

Who builds on its devices?

Later devices cite its devices 3 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K871867Elite Modular Hip SystemThackray USA · 19883cite it

What has FDA decided for it lately?

  • K882890Wroblewski Spring Compression Wire SystemThackray USA · 1988
  • K871867Elite Modular Hip SystemThackray USA · 1988
  • K871852Coxa Acetabular CupThackray USA · 1988
  • K863554Thackray Cruciate Sparing Knee CS-1Thackray USA · 1986
  • K855166Thackray Total Condylar KneesThackray USA · 1986

All 5 as Thackray USA →