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 14, 2026, FDA's public records list DMP with 9 510(k) clearances. The most recent is a 510(k) clearance dated Sep 28, 2012: BRIGHT RESTORATIVE MATERIALS.
| Sep 28, 2012 | BRIGHT RESTORATIVE MATERIALSK121915 · EBF | 510(k) clearances |
| Jan 13, 2011 | BONASIL A+ IMPRESSION MATERIALSK102836 · ELW | 510(k) clearances |
| Dec 3, 2010 | DMP PIT & FISSURE SEALANTK102252 · EBC | 510(k) clearances |
| Nov 23, 2010 | DMP ETCHING GELK102255 · EBF | 510(k) clearances |
| Nov 23, 2010 | DMP SINGLE BONDINGK102254 · KLE | 510(k) clearances |
| Nov 19, 2010 | NANOCERAM- BRIGHTK102257 · EBF | 510(k) clearances |
| Jun 14, 1989 | LATEX EXAM GLOVES (MFG. BROADLAND RUBBER INDUST.)K892965 · LYY | 510(k) clearances |
| Jun 6, 1989 | PATIENT EXAMINATION GLOVES (LATEX)K892150 · LYY | 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
