510(k) Report

FDA applicant

Toshiba Glass Co., Ltd.

Tokyo, 105 Japan, JP1 decision1988–19880 recalls

FDA records 1 decision for Toshiba Glass Co., Ltd. (Tokyo, 105 Japan, JP) in 1988: 1 510(k) clearance. All are in product code FLL (Continuous Measurement Thermometer). 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, general hospital panel, where it files most

How often FDA has decided Toshiba Glass Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Toshiba Glass Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • FLLContinuous Measurement Thermometer1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K881909Toshiba Digital Clinical ThermometerToshiba Glass Co., Ltd. · 19881cites it

What has FDA decided for it lately?

  • K881909Toshiba Digital Clinical ThermometerToshiba Glass Co., Ltd. · 1988

The one decision as Toshiba Glass Co., Ltd. →

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 146Toshiba America Mri, Inc. 68Toshiba Medical Systems 54Toshiba Medical Systems Corporation, Japan 9Toshiba Medical Systems Coporation, Japan 5Toshiba Medical Systems Coroporation 2Toshiba America Electronic Components, Inc. 1