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 Stephens Instruments with 5 510(k) clearances. The most recent is a 510(k) clearance dated Nov 1, 2002: GAYHEART CORNEAL EXCISION DEVICE.
| Date | Record | Source |
|---|---|---|
| Nov 1, 2002 | GAYHEART CORNEAL EXCISION DEVICEK022843 · HRH | 510(k) clearances |
| Nov 1, 2002 | STEPHENS DISPOSABLE FORCEPSK022835 · HNR | 510(k) clearances |
| Nov 1, 2002 | STEPHENS DISPOSABLE HOOKSK022842 · HNQ | 510(k) clearances |
| Nov 1, 2002 | STEPHENS DISPOSABLE SCISSORSK022840 · HNF | 510(k) clearances |
| Nov 1, 2002 | STEPHENS DISPOSABLE SPECULUMK022836 · HNC | 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
