FDA applicant

Mitsubishi Electric Corporation Kyoto Works

Ise-Shi, JP1 decision2006–20060 recalls

FDA records 1 decision for Mitsubishi Electric Corporation Kyoto Works (Ise-Shi, JP) in 2006: 1 510(k) clearance. All are in product code LMC (Camera, Multi Format, Radiological). 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, radiology panel, where it files most

How often FDA has decided Mitsubishi Electric Corporation Kyoto Works’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mitsubishi Electric Corporation Kyoto Works since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Mitsubishi Electric Corporation Kyoto Works by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Mitsubishi”

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

Mitsubishi Intl. Corp. 5 Mitsubishi Kagaku Iatron 4 Mitsubishi Heavy Industries, Ltd. 3 Mitsubishi Electronics America, Inc. 3 Mitsubishi Chemical Medience Corporation 3 Mitsubishi Cable America, Inc. 3 Mitsubishi Yuka America, Inc. 2

Mitsubishi Electric Corporation Kyoto Works

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Mitsubishi”