FDA applicant

Toshiba America Mri, Inc.

S. San Francisco, CA68 decisions1990–20005 recalls

FDA records 68 decisions for Toshiba America Mri, Inc. (S. San Francisco, CA) from 1990 to 2000: 68 510(k) clearances. Most are in product codes LNH (System, Nuclear Magnetic Resonance Imaging) and MOS (Coil, Magnetic Resonance, Specialty). Its devices cite 29 predicates, 23 of them its own earlier devices. 5 recalls are 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 Toshiba America Mri, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Toshiba America Mri, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Toshiba America Mri, Inc.’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 “Toshiba”

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

Toshiba America Medical Systems, In.C 146 Toshiba Medical Systems 54 Toshiba Medical Systems Corporation, Japan 9 Toshiba Medical Systems Coporation, Japan 5 Toshiba Medical Systems Coroporation 2 Toshiba America Electronic Components, Inc. 1 Toshiba Glass Co., Ltd. 1

Toshiba America Mri, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Toshiba”