FDA applicant

Noritake Co., Inc.

Washington, DC14 decisions1989–20110 recalls

FDA records 14 decisions for Noritake Co., Inc. (Washington, DC) from 1989 to 2011: 14 510(k) clearances. All are in product code EIH (Powder, Porcelain). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Noritake Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2011

2007high 2 (2011) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Noritake Co., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Noritake Co., Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?