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 Dantec Electronics, Inc. with 12 510(k) clearances. The most recent is a 510(k) clearance dated Jun 18, 1990: CONCENTRIC ELECTRODE TYPE #13R01, 13R02.
| Date | Record | Source |
|---|---|---|
| Jun 18, 1990 | CONCENTRIC ELECTRODE TYPE #13R01, 13R02K895460 · IKT | 510(k) clearances |
| May 14, 1990 | SENSORY NEEDLE ELECTRODE DNE 111-115,116-117,118K894911 · GXZ | 510(k) clearances |
| Oct 4, 1989 | DANTEC 22K60/61/62 CATHETER TIP TRANSDUCERK884915 · FAP | 510(k) clearances |
| Oct 17, 1988 | DANTEC MAGNETIC STIMULATORK881915 · GWF | 510(k) clearances |
| Apr 14, 1988 | 13L81 DISPOSABLE SPHINCTER ELECTRODE, 13L33 CABLEK874759 · FAP | 510(k) clearances |
| Apr 14, 1988 | DANTEC 13L40 ST. MARKS'S PUDENDAL ELECTRODEK874758 · FAP | 510(k) clearances |
| Jan 22, 1988 | DANTEC 13L35/36/37 STIM. AND RECORDING ELECTRODEK874735 · GXY | 510(k) clearances |
| Oct 6, 1987 | EVOPORT 300K870567 · GWF | 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
