Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Meridian Co., Ltd. with 13 510(k) clearances. The most recent is a 510(k) clearance dated Jan 25, 2024: MR Q; MR Q SUPINE; MR Q SLT.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Jan 25, 2024 | MR Q; MR Q SUPINE; MR Q SLTK232417 · HQF | 510(k) clearances |
| Sep 12, 2023 | Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulseK231011 · HQF | 510(k) clearances |
| May 19, 2017 | MICRORUPTOR 6K160677 · GEX | 510(k) clearances |
| Feb 14, 2012 | LASER INDIRECT OPHTHALMOSCOPE 500(LIO-500)K113390 · GEX | 510(k) clearances |
| Feb 25, 2011 | LUCIAK102375 · ILY | 510(k) clearances |
| Dec 29, 2008 | LAPEX BCSK081962 · ILY | 510(k) clearances |
| Dec 14, 2007 | MERILAS 532AK072823 · HQF | 510(k) clearances |
| Jan 21, 2005 | LAPEX 2000K034009 · NHN | 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
