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 15, 2026, FDA's public records list Medical Devices, Inc. with 50 510(k) clearances. The most recent is a 510(k) clearance dated Oct 30, 2013: OPHTHALMOSCOPES DIAGNOSTIC INSTRUMENT KITS.
| Oct 30, 2013 | OPHTHALMOSCOPES DIAGNOSTIC INSTRUMENT KITSK131719 · HLJ | 510(k) clearances |
| Feb 5, 2001 | PAD PRO PEDIATRIC ELECTRODE, MODEL PAD PRO 2602K002280 · MKJ | 510(k) clearances |
| Sep 1, 1995 | MICRO-ARTHROSCOPEK930084 · HRX | 510(k) clearances |
| Dec 5, 1994 | SMARTBRACE ELECTRODEK940012 · GXY | 510(k) clearances |
| Dec 5, 1994 | ELECTROFLEXK943126 · GXY | 510(k) clearances |
| Mar 14, 1994 | HOME MICROCURRENT HMCK935132 · GZJ | 510(k) clearances |
| Feb 23, 1994 | FLEXMATEK934619 · GZJ | 510(k) clearances |
| Jul 6, 1993 | XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300K924897 · GCT | 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
