Medical device 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 CMT Medical Technologies with 12 510(k) clearances. The most recent is a 510(k) clearance dated Sep 3, 2020: ArtPIX DRF.
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.
| Sep 3, 2020 | ArtPIX DRFK202235 · JAA | 510(k) clearances |
| Sep 22, 2016 | ArtPix Mobile EZ2GOK162224 · KPR | 510(k) clearances |
| Apr 26, 2011 | PRESTODR 4143K110849 · KPR | 510(k) clearances |
| Mar 29, 2011 | DUET DRFK103038 · JAA | 510(k) clearances |
| Apr 22, 2010 | PRESTODR PORTABLEK100400 · IZL | 510(k) clearances |
| Apr 29, 2008 | SMARTSPOT PRIMAXK080890 · LLZ | 510(k) clearances |
| Jul 3, 2001 | SMART RADK003438 · MQB | 510(k) clearances |
| Jul 7, 2000 | PANORET, MODEL 1000AK001111 · HKL | 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
