Diagnostics makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Biovision with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 16, 2004: MODIFICATION TO VISITOME 20-10 MICROKERATOME.
| Nov 16, 2004 | MODIFICATION TO VISITOME 20-10 MICROKERATOMEK042083 · HNO | 510(k) clearances |
| Mar 11, 2002 | VISTITOME 20-10 MICROKERATOMEK014000 · HNO | 510(k) clearances |
| Jan 30, 1998 | LEADFIX BIORESORBABLE MEMBRANCE PIN SYSTEMK974392 · DZL | 510(k) clearances |
| Sep 14, 1993 | B-SCAN OPTHALMIC ULTRASOUND IMAGING SYSTEMK926251 · IYO | 510(k) clearances |
| Sep 25, 1991 | CRYSTAL FOCUS EMERALD LASER SLT MCX 1.5 CONVEX PROK910027 · GEX | 510(k) clearances |
| Jun 22, 1990 | DIAMOND ND:YAG OPHTHALMIC LASERK901636 · GEX | 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
