Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ChinaLabelled 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 13, 2026, FDA's public records list Minxray with 18 510(k) clearances. The most recent is a 510(k) clearance dated Mar 19, 2021: IMPACT and X-Ranger.
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 |
|---|---|---|
| Mar 19, 2021 | IMPACT and X-RangerK210479 · IZL | 510(k) clearances |
| Jul 8, 2020 | CMDR 2C (Multiple Models)K201575 · IZL | 510(k) clearances |
| Jul 3, 2019 | CMDR 2CW (Multiple models)K191451 · IZL | 510(k) clearances |
| Dec 14, 2018 | TR90BHK182207 · IZL | 510(k) clearances |
| Jun 7, 2017 | CMDR 2ST (Multiple Models), CMDR 2SPE (Multiple Models), IntegrisK171353 · IZL | 510(k) clearances |
| Feb 2, 2016 | HF1202H PowerPlus Portable X-ray EquipmentK153059 · IZL | 510(k) clearances |
| Sep 18, 2014 | CMDR-2ST & CMDR-2SLWT DIGITAL PORTABLE X-RAYK141885 · IZL | 510(k) clearances |
| May 12, 2010 | MINXRAY, MODEL: BPD60K091255 · EHD | 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
