Medical device makerLabelled 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 15, 2026, FDA's public records list Hayes Medical, Inc. with 12 510(k) clearances. The most recent is a 510(k) clearance dated Jan 31, 2007: 36MM COCR FEMORAL HEAD AND 36MM ACETABULAR INSERT.
| Jan 31, 2007 | 36MM COCR FEMORAL HEAD AND 36MM ACETABULAR INSERTK070061 · LWJ | 510(k) clearances |
| Dec 21, 2006 | UNISYN HA PLASMA MODULAR HIPK062383 · LWJ | 510(k) clearances |
| Apr 28, 2006 | CONSENSUS ACETABULAR SHELL SYSTEMK060635 · LPH | 510(k) clearances |
| Apr 10, 2003 | CONSENSUS HIP SYSTEM, UNISYN HIP SYSTEMK030151 · LZO | 510(k) clearances |
| Apr 1, 2003 | CONSENSUS UNIPOLAR HEAD, COCRK030205 · KWL | 510(k) clearances |
| Jul 24, 2002 | CONSENSUS ACETABULAR INSERT, CROSS-LINKED POLYETHYLENEK021466 · LPH | 510(k) clearances |
| Apr 15, 2002 | CONSENSUS ACETABLAR SHELL, TI COATEDK020153 · LPH | 510(k) clearances |
| Feb 23, 2001 | TRITON HIP SYSTEMK003649 · LWJ | 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
