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Toshiba Medical Systems Corporation, Japan

Also registered as Toshiba Medical Systems Coporation, Japan

Country not established

Devices
14

What Toshiba Medical Systems Corporation, Japan makes

Toshiba Medical Systems Corporation manufactures magnetic resonance imaging (MRI) systems, including the Vantage Titan 3T series with M-Power GX technology and the OCTAVE SpeedER head and spine modules, designed for high-resolution imaging. The company also produces diagnostic ultrasound systems like the APLIO ARTIDA and APLIO XG, as well as computed tomography (CT) scanners such as the AQUILION Premium. Additionally, it offers specialized imaging software, including SureSubtraction Lung for enhanced lung imaging analysis.

These devices are classified under Class II in the United States and are listed in the FDA’s 510(k) registry. The company operates with a US-based presence, though its headquarters remain in Japan.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue14

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  • Vantage Titan 3T, MRT-3010/A7, M-Power GX Ref K172878 Open recall

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Aplio Artida Diagnostic Ultrasound System Ref K121577

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Vantage Titan 3T Ref K102489

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • 4CH Flex Speeder Ref K112366

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Kalare Diagnostic X-Ray Table System Ref K110785

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Octave Speeder Head Ref K121910

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Infinix Cf-I/Sp And Infinix Vf-I/Sp Model Infx-8000V Ref K112054

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Aplio 500/400/300 Diagnostic Ultrasound System Ref K121422

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Octave Speeder Spine Ref K121911

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Suresubtraction Lung Ref K133324

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Aplio Xg Diagnostic Ultrasound System Ref K103645

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • 4CH Flex Speeder Ref K111251

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Aquilion One Ref K113466

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Aquilion Premium Ref K120546 Open recall

    Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 1-14 of 14

Frequently asked questions

How many devices does Toshiba Medical Systems Corporation, Japan have in the registry?

The registry currently lists 14 devices for Toshiba Medical Systems Corporation, Japan. Devices recorded under merged duplicate company entries are counted once.

Which registries list Toshiba Medical Systems Corporation, Japan's devices?

Among its 14 most recently registered devices, Toshiba Medical Systems Corporation, Japan has devices listed in FDA 510(k) (14 devices).

What risk classes do Toshiba Medical Systems Corporation, Japan's devices fall under?

Among its 14 most recently registered devices, the classes recorded for Toshiba Medical Systems Corporation, Japan's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Toshiba Medical Systems Corporation, Japan in the registry?

The most recently registered devices listed for Toshiba Medical Systems Corporation, Japan include Vantage Titan 3T, MRT-3010/A7, M-Power GX, APLIO ARTIDA DIAGNOSTIC ULTRASOUND SYSTEM, VANTAGE TITAN 3T and 4CH FLEX SPEEDER.

Generated automatically from registry data and not verified by a human reviewer.