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 Eagle Vision with 7 510(k) clearances. The most recent is a 510(k) clearance dated May 2, 2006: EAGLEVISION GELLANSERTS, MODEL REF 0040.
| May 2, 2006 | EAGLEVISION GELLANSERTS, MODEL REF 0040K053333 · LZU | 510(k) clearances |
| Apr 25, 2003 | MONOCANALICULAR STENTS, LACRIMAL INTUBATION SETSK030353 · OKS | 510(k) clearances |
| Apr 20, 1999 | FLEXPLUGK991130 · LZU | 510(k) clearances |
| Jun 6, 1991 | EAGLE VISION FREEMAN RADIOPAGUE PUNCTUM PLUGK905427 · LZU | 510(k) clearances |
| May 16, 1989 | TEMPORARY INTRACANALICULAR COLLAGEN IMPLANTK890919 · LZU | 510(k) clearances |
| Apr 11, 1989 | EAGLE VISION-FREEMAN(TM) PUNCTAL VALVEK890920 · LZU | 510(k) clearances |
| Aug 22, 1988 | EV MONOCANALICULAR STENT (TM)K883233 · OKS | 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
