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 15, 2026, FDA's public records list Foremost Dental Manufacturing with 15 510(k) clearances. The most recent is a 510(k) clearance dated Aug 10, 1998: ZENITH LUXACORE AUTOMIX CORE MATERIAL (MULTIPLE).
| Aug 10, 1998 | ZENITH LUXACORE AUTOMIX CORE MATERIAL (MULTIPLE)K982201 · EBF | 510(k) clearances |
| Jul 10, 1998 | PERMACEM AUTOMIX LUTING CEMENT SYSTEMK981813 · EBF | 510(k) clearances |
| May 11, 1998 | HONIGUM AUTOMIX IMPRESSION MATERIAL (FOIL BAGS) AND HONIGUM QUICK IMPRESSION MATERIAL (CARTRIDGES)K980963 · ELW | 510(k) clearances |
| Jul 15, 1997 | ZENTIH FLOWABLE COMPOSITE (MULTIPLE)K970683 · EBF | 510(k) clearances |
| Jun 3, 1997 | TEMPOCEM NE (MULTIPLE)K970774 · EMA | 510(k) clearances |
| Jun 3, 1997 | TEMPO CEM (MULTIPLE)K970775 · EMA | 510(k) clearances |
| Mar 8, 1996 | IONOSIT SEALK954867 · EBC | 510(k) clearances |
| Jan 21, 1994 | IONOSIT BASE LINERK935689 · EBD | 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
