Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Den-Mat Corp. with 29 510(k) clearances and 1 drug application. The most recent is a 510(k) clearance dated Feb 9, 1999: 1ST IMPRESSION.
| Feb 9, 1999 | 1ST IMPRESSIONK983106 · ELW | 510(k) clearances |
| Aug 3, 1990 | DEN-MAT CERINATE PORCELAINK895731 · EIH | 510(k) clearances |
| Feb 22, 1990 | DEN-MAT LAMI-QUICKK895269 · ELL | 510(k) clearances |
| Jul 15, 1988 | LIGHT-CURED ZIONOMER CEMENTK881918 · EMA | 510(k) clearances |
| Mar 18, 1988 | DEN-MAT PORETCH (PORCELAIN ETCHANT)K875351 · ELL | 510(k) clearances |
| Aug 24, 1987 | DEN-MAT TENUREK872510 · EBF | 510(k) clearances |
| Feb 19, 1987 | DEN-MAT SECURE ANTI-ROTATIONAL POST-CORE SYSTEMK870130 · ELR | 510(k) clearances |
| Jan 7, 1987 | REMBRANDT PORCELAIN TINTING KITK864346 · EBF | 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
