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., part of DentaurumLabelled 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 Dentauraum, Inc. with 24 510(k) clearances. The most recent is a 510(k) clearance dated Jul 27, 1995: REMATITAN TITANIUM.
| Jul 27, 1995 | REMATITAN TITANIUMK952866 · EJH | 510(k) clearances |
| Jul 27, 1995 | REMANIUM: CS & G-SOFTK952870 · EJH | 510(k) clearances |
| Jul 27, 1995 | REMANIUM:GM 700, GM 380, GM 800, GFHK952867 · EJH | 510(k) clearances |
| Jul 26, 1995 | REMANIUM: 200,CS, 380, AND CDK952865 · EJH | 510(k) clearances |
| Jul 19, 1995 | DENTAURUM JACKET CROWN & ROOT POSTSK952868 · EBL | 510(k) clearances |
| Feb 13, 1995 | DENT-O-CRYL ORTHODONTIC ACRYLICK942667 · KMY | 510(k) clearances |
| Aug 10, 1994 | ORTHALGENAT IMPRESSION MATERIALK942666 · ELW | 510(k) clearances |
| Aug 1, 1994 | EXTRAORAL HEADGEARK936151 · DZB | 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
