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 Johnson & JohnsonLabelled 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. See the Johnson & Johnson group view.
As of Nov 15, 2026, FDA's public records list Mentor O&O with 18 510(k) clearances. The most recent is a 510(k) clearance dated Feb 12, 1996: MENTOR MERIDIAN PHACOEMULSIFICATION SYSTEM.
| Feb 12, 1996 | MENTOR MERIDIAN PHACOEMULSIFICATION SYSTEMK955245 · HQC | 510(k) clearances |
| Feb 16, 1994 | MENTOR WET-FIELD HEMOSTATIC ERASER BIPOLAR INSTRUMENT, 20 GAUGE WITH EXTRUSION ASPIRATIONK934320 · HQR | 510(k) clearances |
| Jun 11, 1992 | MENTOR ODYSSEY PHACOEMULSIFICATION SYSTEMK912904 · HQC | 510(k) clearances |
| Mar 30, 1992 | MENTOR HORIZON LOW VISION MAGNIFIERK915340 · HJG | 510(k) clearances |
| May 13, 1991 | MENTOR(R) SUR-E-TROL(R)K910637 · FRN | 510(k) clearances |
| May 2, 1991 | MENTOR(R) WET-FIELD(R) II AC COAGULATOR, 22-1305K911160 · GEI | 510(k) clearances |
| Nov 5, 1990 | MENTOR(R) DURASTAT(TM) AUTOCLAV BIPOLAR HEMOSTATK903878 · HQQ | 510(k) clearances |
| Sep 11, 1989 | MENTOR SPECTACLE BINOCULAR INDIRECT OPHTHALMOSCOPEK895010 · HLI | 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
