FDA applicant

Kyocera Corporation

Kyoto, JP1 decision2024–20240 recalls

FDA records 1 decision for Kyocera Corporation (Kyoto, JP) in 2024: 1 510(k) clearance. All are in product code LZO (Prosthesis, Hip, Semi-Constrained…). Its devices cite 1 predicate, 0 of them its own earlier devices. 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, orthopedic panel, where it files most

How often FDA has decided Kyocera Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2024high 1 (2024) · low 0 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2024.

FIG. 1 — Kyocera Corporation by year, 2024–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Kyocera Corporation’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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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 International, Inc. 3 Kyocera America, Inc. 1 Kyocera Medical Corporation 1

Kyocera Corporation

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Kyocera”