Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Thackray USA with 5 510(k) clearances. The most recent is a 510(k) clearance dated Aug 8, 1988: WROBLEWSKI SPRING COMPRESSION WIRE SYSTEM.
| Date | Record | Source |
|---|---|---|
| Aug 8, 1988 | WROBLEWSKI SPRING COMPRESSION WIRE SYSTEMK882890 · JDQ | 510(k) clearances |
| Apr 8, 1988 | ELITE MODULAR HIP SYSTEMK871867 · JDI | 510(k) clearances |
| Feb 18, 1988 | COXA ACETABULAR CUPK871852 · JDI | 510(k) clearances |
| Oct 6, 1986 | THACKRAY CRUCIATE SPARING KNEE CS-1K863554 · | 510(k) clearances |
| Mar 13, 1986 | THACKRAY TOTAL CONDYLAR KNEESK855166 · JWH | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
