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 15, 2026, FDA's public records list Magnivision with 8 510(k) clearances. The most recent is a 510(k) clearance dated Mar 30, 1990: ITEM #273 CONTACT LENS CASES.
| Mar 30, 1990 | ITEM #273 CONTACT LENS CASESK900777 · LRX | 510(k) clearances |
| Mar 30, 1990 | ITEM #272 MAGNIF-EYES CONTACT LENS CASEK900778 · LRX | 510(k) clearances |
| Feb 28, 1990 | CONFEES(R)+ CONTACT LENS HOLDERK897084 · LRX | 510(k) clearances |
| Feb 28, 1990 | COMFEES(R) + CON-PAK(TM) LENS CASEK897085 · LRX | 510(k) clearances |
| Jun 23, 1989 | DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283K882384 · LRX | 510(k) clearances |
| Jun 23, 1989 | ITEM #352/#CS352* CONTACT LENS CASESK890533 · LRX | 510(k) clearances |
| Aug 10, 1987 | SOFT CONTACT LENS REMOVERK872567 · KYE | 510(k) clearances |
| Aug 4, 1987 | HARD CONTACT LENS REMOVER. ITEM #289K872591 · KYE | 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
