Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Becton DickinsonLabelled by claude-sonnet-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 Visitec Company with 49 510(k) clearances. The most recent is a 510(k) clearance dated Oct 12, 1995: VISITEC COLLAR BUTTON CATHETER {GRIFFITHS}.
| Oct 12, 1995 | VISITEC COLLAR BUTTON CATHETER {GRIFFITHS}K953394 · LZU | 510(k) clearances |
| Feb 23, 1995 | VISITEC SCLERAL PLUGK945114 · LXP | 510(k) clearances |
| Feb 14, 1995 | VISIFLEX OPHTHALMIC SURGICAL INCISE DRAPEK945738 · HMT | 510(k) clearances |
| Jan 17, 1995 | VISITEC SILICONE RETINAL IMPLANTS/EXPLANTSK945172 · HQX | 510(k) clearances |
| Jul 12, 1994 | VISITEC PRECISE-POINTK942234 · GAP | 510(k) clearances |
| May 17, 1994 | FIBEROPTIC ILLUMINATED INSTRUMENTSK934269 · HJM | 510(k) clearances |
| Mar 7, 1994 | VISITEC EYE PADK940210 · EFQ | 510(k) clearances |
| Dec 27, 1993 | VISI-SPEAR EYE SPONGEK933872 · HOZ | 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
