Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of MeniconLabelled 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 Menicon U.S.A. with 3 510(k) clearances. The most recent is a 510(k) clearance dated May 19, 2000: MENICON Z.
| May 19, 2000 | MENICON ZK000133 · HQD | 510(k) clearances |
| Aug 22, 1997 | MENICON SF-P AND MENICON Z RIGID GAS PERMEABLE CONTACT LENSK972443 · HQD | 510(k) clearances |
| Mar 25, 1997 | MENICON Z BIFOCAL DESIGN LENS/MENICON Z TRIFOCAL DESIGN LENSK970019 · LPL | 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
