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 13, 2026, FDA's public records list Simpson/Basye, Inc. with 12 510(k) clearances. The most recent is a 510(k) clearance dated Mar 25, 1994: SEDLACEK HANDLE.
| Date | Record | Source |
|---|---|---|
| Mar 25, 1994 | SEDLACEK HANDLEK926179 · HGI | 510(k) clearances |
| Jun 23, 1989 | MARLOW ANAL SPECULUMK891352 · KOA | 510(k) clearances |
| May 11, 1989 | NEWPORT LATERAL VAGINAL RETRACTORK891351 · KOH | 510(k) clearances |
| Mar 29, 1989 | REID ENDOCERVICAL SPREADERK891347 · HDC | 510(k) clearances |
| Mar 29, 1989 | NEWPORT CERVICAL MANIPULATORK891350 · HDC | 510(k) clearances |
| Mar 29, 1989 | CAMPION CERVICAL HOOKK891349 · HDC | 510(k) clearances |
| Mar 22, 1989 | CAMPION LASER FORCEPSK891348 · GEN | 510(k) clearances |
| May 7, 1987 | HEATED INSTRUMENT BATHK870276 · LRJ | 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
