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 Ivoclar VivadentLabelled 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 Ivoclar USA, Inc. with 11 510(k) clearances. The most recent is a 510(k) clearance dated Nov 21, 2001: HIGH GOLD PALLADIUM FREE CERAMIC SOLDER.
| Nov 21, 2001 | HIGH GOLD PALLADIUM FREE CERAMIC SOLDERK012877 · EJT | 510(k) clearances |
| Jul 2, 1998 | ARISTON PHCK981264 · EBF | 510(k) clearances |
| May 11, 1998 | PROCADK980986 · EIH | 510(k) clearances |
| Aug 17, 1994 | PROVIPONT C&BK941849 · EBG | 510(k) clearances |
| Nov 4, 1992 | DW243-64K923644 · EJS | 510(k) clearances |
| Feb 25, 1987 | SR 3/60 NF DENTURE MATER. & SELF-CURE DENT. RESINK864708 · EBI | 510(k) clearances |
| Feb 10, 1987 | SR-VIVODENT ANTERIOR & SR-ORTHOTYP POSTERIOR TEETHK864707 · ELM | 510(k) clearances |
| Feb 10, 1987 | IVOCRYL HEAT CURE & IVOCRYL QUICK DENTURE MATERIALK864709 · EBI | 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
