FDA applicant

Kyocera International, Inc.

San Diego, CA3 decisions1976–19860 recalls

FDA records 3 decisions for Kyocera International, Inc. (San Diego, CA) from 1976 to 1986: 3 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and 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 Kyocera International, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kyocera International, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Kyocera”

FDA records each applicant name separately; these may or may not be the same firm.

Kyocera Medical Technologies, Inc. 16 Kyocera Medical Technologies Inc. (KMTI) 3 Kyocera Corporation 1 Kyocera America, Inc. 1 Kyocera Medical Corporation 1

Kyocera International, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Kyocera”