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 Dyn-A-Med Products with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 17, 1984: CLAMP, TUBING, LINE.
| Dec 17, 1984 | CLAMP, TUBING, LINEK844121 · FKK | 510(k) clearances |
| Dec 29, 1981 | GEL ELECTRODEK813176 · DRX | 510(k) clearances |
| May 27, 1981 | BLADE, TONGUEK811157 · | 510(k) clearances |
| Nov 24, 1980 | PLASTIC ADHESIVE BANDAGEK802764 · KGX | 510(k) clearances |
| Oct 31, 1980 | SPATULA, CERVICAL CYTOLOGICAL CYTOLOGYK802139 · HHT | 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
