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 14, 2026, FDA's public records list Medart Corp. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jun 13, 2012: MEDART 620.
| Jun 13, 2012 | MEDART 620K120573 · GEX | 510(k) clearances |
| Jun 28, 2011 | MEDART DIODE LASER SYSTEM & ACCESSORIESK110243 · GEX | 510(k) clearances |
| Nov 24, 2009 | MEDART MODEL 610 CO2 LASER SYSTEM & ACCESSORIESK083123 · GEX | 510(k) clearances |
| Jun 7, 2001 | UNI-LASER 470K010885 · GEX | 510(k) clearances |
| May 15, 2000 | MEDART 520 COOLING SYSTEMK000503 · GEX | 510(k) clearances |
| May 11, 2000 | UNI-LASER 430K993815 · GEX | 510(k) clearances |
| Jul 29, 1999 | UNI-LASER 425P DIODE LASER SYSTEM & ACCESSORIESK991659 · GEX | 510(k) clearances |
| Jul 12, 1999 | UNI-LASER 450P CO2 LASER SYSTEM & ACCESSORIESK991297 · GEX | 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
