Medical device makerLabelled 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 14, 2026, FDA's public records list Noritake Co., Inc. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Aug 12, 2011: ZIRPRIME.
| Aug 12, 2011 | ZIRPRIMEK111383 · EIH | 510(k) clearances |
| Jun 30, 2011 | SUPER PORCELAIN EX-3 UNIVERSAL OPAQUEK111107 · EIH | 510(k) clearances |
| Nov 23, 2005 | SUPER PORCELAIN EX-3 PRESSK052304 · EIH | 510(k) clearances |
| May 11, 2005 | CZR PRESS LF STAINSK050920 · EIH | 510(k) clearances |
| Feb 7, 2005 | KATANA ZIRCONIAK050160 · EIH | 510(k) clearances |
| Jan 11, 2005 | CZR PRESS LFK043462 · EIH | 510(k) clearances |
| Dec 22, 2003 | CERABIEN ZRK031968 · EIH | 510(k) clearances |
| Oct 24, 2003 | CZR PRESSK033049 · EIH | 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
