Diagnostics 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 Mira with 21 510(k) clearances. The most recent is a 510(k) clearance dated Mar 19, 1997: SCHEPENS-YOSHIDA VIDEO BINOCULAR INDIRECT OPHTHALMSCOPE.
| Mar 19, 1997 | SCHEPENS-YOSHIDA VIDEO BINOCULAR INDIRECT OPHTHALMSCOPEK951728 · HLI | 510(k) clearances |
| Jun 5, 1996 | SOLID DILICONE IMPLANTS, SDILICONE SPONGE IMPLANTSK950806 · HQX | 510(k) clearances |
| Jul 15, 1994 | RETURN PATH DIATHERMY HANDLEK941495 · HQR | 510(k) clearances |
| Jan 25, 1994 | MODIFICATION OF ANTERIOR SEGMENT ELECTRODESK933527 · HWA | 510(k) clearances |
| Oct 19, 1992 | OPHTHALMIC TRICHIASIS PROBEK923629 · HPS | 510(k) clearances |
| Feb 27, 1990 | CONVERTER SYSTEMK894248 · HQE | 510(k) clearances |
| May 23, 1989 | POWER OPERATED AND CONTROLLED VITREOUS SCISSORSK891601 · HQE | 510(k) clearances |
| May 8, 1989 | LIGHT SOURCE, ENDOSCOP, XENON ARCK890448 · FFS | 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
