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Siemens Medical Laboratories, Inc.

United StatesFDA applicant, unverified

Devices
13

What Siemens Medical Laboratories, Inc. makes

The company manufactures medical linear accelerators, including the MEVATRON series (models M 2, 74X, KD-2, 67, 67E, and ME), designed for external beam radiation therapy. It also produces radiation therapy treatment tables (e.g., Z XT) and ultrasound imaging systems (e.g., SONOLINE CF). Additional offerings include patient data management systems (Project 735) and treatment planning software like BEAMVIEW and BEAMVIEW PLUS (Project 743).

These devices are classified as Class II under FDA regulations and are recorded in the 510(k) clearance database. The company is based in the United States.

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

Catalogue13

Newest first, rows 1-13 of 13

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  • Mevatron, M 2 Class Ref K882729

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

  • Z Xt Radiation Therapy Treatment Table Ref K910971

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

  • Sonoline Cf Ref K875272

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

  • Mevatron 74X Medical Linear Accelerator Ref K791967

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

  • Mevatron Kd-2 Ref K862339

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

  • Mevatron 67 Ref K790688

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

  • Mevatron 60 Ref K790388

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

  • Mevatron 67E Ref K812032

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

  • Patient Data Management System (Project 735) Ref K894230

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

  • Mevamatic 3 Ref K854609

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

  • Beamview & Beamview Plus (Aka Project 743) Ref K903139

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

  • Siemens Mevatron Me Ref K852907

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

  • Mevatron 74 Ref K790747

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

Rows 1-13 of 13

Frequently asked questions

How many devices does Siemens Medical Laboratories, Inc. have in the registry?

The registry currently lists 13 devices for Siemens Medical Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Siemens Medical Laboratories, Inc.'s devices?

Among its 13 most recently registered devices, Siemens Medical Laboratories, Inc. has devices listed in FDA 510(k) (13 devices).

What risk classes do Siemens Medical Laboratories, Inc.'s devices fall under?

Among its 13 most recently registered devices, the classes recorded for Siemens Medical Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Siemens Medical Laboratories, Inc. in the registry?

The most recently registered devices listed for Siemens Medical Laboratories, Inc. include MEVATRON, M 2 CLASS, Z XT RADIATION THERAPY TREATMENT TABLE, SONOLINE CF and MEVATRON 74X MEDICAL LINEAR ACCELERATOR.

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