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 14, 2026, FDA's public records list Cedar Surgical with 17 510(k) clearances. The most recent is a 510(k) clearance dated Dec 17, 1987: RAYLOR(TM) DRILL STOP.
| Dec 17, 1987 | RAYLOR(TM) DRILL STOPK873692 · HBE | 510(k) clearances |
| Nov 2, 1987 | RAYLOR FUSION FUNNELK872281 · HXR | 510(k) clearances |
| Oct 26, 1987 | CEDAR(TM) PELVIC CUSHIONK873690 · LWG | 510(k) clearances |
| Sep 28, 1987 | CEDAR(TM) RETRACTOR RINGK873691 · GZT | 510(k) clearances |
| Dec 12, 1986 | RAYLOR(TM) DISSECTING HOOKK864425 · GDG | 510(k) clearances |
| Nov 26, 1986 | RAYLOR(TM) DEPTH GAUGEK864426 · HTJ | 510(k) clearances |
| Nov 26, 1986 | RAYLOR(TM) PROTECTIVE RETRACTORK864424 · GAD | 510(k) clearances |
| Nov 26, 1986 | RAYLOR(TM) PERIOSTEAL ELEVATORSK864421 · GEG | 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
