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 13, 2026, FDA's public records list NDM Corp. with 11 510(k) clearances. The most recent is a 510(k) clearance dated May 12, 1993: CLEARSITE STERILE WOUND DRESSING, NDM WOUND DRESSI.
| Date | Record | Source |
|---|---|---|
| May 12, 1993 | CLEARSITE STERILE WOUND DRESSING, NDM WOUND DRESSIK926202 · NAE | 510(k) clearances |
| May 9, 1990 | NDM SWITCHPEN HOLSTERK901145 · GEI | 510(k) clearances |
| Nov 14, 1985 | DIATEMP ELECTROSURGICAL PENK853968 · GEI | 510(k) clearances |
| Apr 28, 1983 | PENCIL SKIN ABRADERK830663 · DRX | 510(k) clearances |
| May 1, 1981 | NDM DIATEMP INFANT ELECTROSURG. DISP. P.K810920 · HAM | 510(k) clearances |
| May 23, 1980 | NDM DIATEMP ELECTROSURGICAL DIS. PADK801158 · GEI | 510(k) clearances |
| Apr 26, 1979 | NDM PAPER TAPE ECG ELECTRODEK790730 · DRX | 510(k) clearances |
| Jan 31, 1978 | I.V. CATHETERK772354 · FOZ | 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
