FDA applicant

Mitsubishi Intl. Corp.

Conshohocken, PA5 decisions1988–19960 recalls

FDA records 5 decisions for Mitsubishi Intl. Corp. (Conshohocken, PA) from 1988 to 1996: 5 510(k) clearances. All are in product code IYE (Accelerator, Linear, Medical). 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 Intl. Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mitsubishi Intl. Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Mitsubishi Intl. Corp. 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 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 1

Mitsubishi Intl. Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Mitsubishi”