Skip to content

Larsen & Toubro Limited

Country not established

Devices
18

What Larsen & Toubro Limited makes

Larsen & Toubro Limited manufactures Class II medical monitoring systems, including portable and modular units like the SKYLINE 55, STAR series (50 N, 55, and Lunar Series), PLANET series (50, 55, and Model 100), and STELLAR models (300 and 404/404T). These devices are designed for real-time patient monitoring, supporting functions such as vital sign tracking and diagnostic data acquisition.

The company’s portfolio is regulated under the FDA’s 510(k) clearance process, with all listed devices classified as Class II. These products are registered in the FDA’s 510(k) database, adhering to U.S. medical device regulations. The manufacturer operates from the United States.

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

Catalogue18

Newest first, rows 1-18 of 18

Search and filter all 18 devices
Skip device list

  • Skyline 55 Ref K081552

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

  • Star 50 N Ref K103686

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

  • Planet 55, Model 100 Ref K090443

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

  • Star 55 Ref K080173

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

  • Planet 55 Ref K071472

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

  • Stellar 404 Monitoring System Ref K042560

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

  • Star (Lunar Series) Monitoring System Ref K032867

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

  • Planet Monitoring System Ref K032871

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

  • Stellar 404T Ref K060058

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

  • Planet 50 Monitoring System Ref K043370

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

  • Stellar 300 Ref K103763

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

  • Star 55 Model 100 Ref K090172

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

  • Galaxy Ref K061816

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

  • Skyline 55, Model Ver 1 Ref K092153

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

  • Stellar 300 Ref K093017

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

  • Star 50 Monitoring System Ref K051608

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

  • Galaxy 55 Ref K082685

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

  • Larsen & Toubro Limited Senorita Color Doppler Ultrasound System Ref K040409

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

Rows 1-18 of 18

Frequently asked questions

How many devices does Larsen & Toubro Limited have in the registry?

The registry currently lists 18 devices for Larsen & Toubro Limited. Devices recorded under merged duplicate company entries are counted once.

Which registries list Larsen & Toubro Limited's devices?

Among its 18 most recently registered devices, Larsen & Toubro Limited has devices listed in FDA 510(k) (18 devices).

What risk classes do Larsen & Toubro Limited's devices fall under?

Among its 18 most recently registered devices, the classes recorded for Larsen & Toubro Limited's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Larsen & Toubro Limited in the registry?

The most recently registered devices listed for Larsen & Toubro Limited include SKYLINE 55, STAR 50 N, PLANET 55, MODEL 100 and STAR 55.

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