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Life Science Instrumentation, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
20

What Life Science Instrumentation, Inc. makes

Life Science Instrumentation, Inc. manufactures electrocardiogram (ECG) monitors, defibrillators, and portable resuscitation systems, including standalone units and those integrated with electrode plates. Their portfolio includes handheld defibrillators (e.g., MINI-DEFIBRILLATOR 280/4), multi-channel ECG recorders (e.g., LIFE TRACE 40/42), and central monitoring devices (e.g., CENTERAL MONITOR 360). Some products combine monitoring and defibrillation capabilities, such as the LS-260G MONITOR/RECORDER & DEFIBILLATOR, while others focus on continuous patient observation (e.g., LIFE WATCH LSI). The company also supplies specialized ECG analysis tools like the CARDIORATER series (CR-3, CR-5, CR-7, CR-9).

The company’s devices are classified under Class II in the U.S. regulatory framework, requiring 510(k) clearance through the FDA’s premarket notification process. Products are listed in the FDA 510(k) database, reflecting their authorised status for commercial distribution. The manufacturer operates from the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue20

Newest first, rows 1-20 of 20

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  • Ls-260g Monitor/Recorder & Defibillator Ref K843396

    Class II
    Active 510(k) 510(k) II

  • Pioneer Ii Back Plate Electrode Ref K820122

    Class II
    Active 510(k) 510(k) II

  • Mini-Defibrillator 280/4 Ref K840246

    Class II
    Active 510(k) 510(k) II

  • Cardiorater Cr-3 Ref K812145

    Class II
    Active 510(k) 510(k) II

  • 280/4 Mini-Defibrillator Ref K812520

    Class II
    Active 510(k) 510(k) II

  • Cardiorater Cr-7 Ref K812147

    Class II
    Active 510(k) 510(k) II

  • 2000 Series Portable Resuscitation Syst. Ref K812519

    Class II
    Active 510(k) 510(k) II

  • Centeral Monitor 360 Ref K812144

    Class II
    Active 510(k) 510(k) II

  • Cr-9 Ref K821223

    Class II
    Active 510(k) 510(k) II

  • Life Trace 40/42 Ref K822389

    Class II
    Active 510(k) 510(k) II

  • Cardiorater Cr-5 Ref K812146

    Class II
    Active 510(k) 510(k) II

  • Life Watch Lsi Ref K822615

    Class II
    Active 510(k) 510(k) II

  • Life Trace 24 Ref K822390

    Class II
    Active 510(k) 510(k) II

  • Defibrillator Vpd 545 Ref K831056

    Class II
    Active 510(k) 510(k) II

  • Emergipace - External Pacemaker Ref K850812

    Class II
    Active 510(k) 510(k) II

  • VPD540 Defibrillator Ref K822617

    Class II
    Active 510(k) 510(k) II

  • Vpd-261 Defibrillator Monitor Ref K822294

    Class II
    Active 510(k) 510(k) II

  • Life Trace 14 Ref K822388

    Class II
    Active 510(k) 510(k) II

  • LS6 Arrythmia Discriminator Ref K822616

    Class II
    Active 510(k) 510(k) II

  • Ls 5 Ref K842037

    Class II
    Active 510(k) 510(k) II

Rows 1-20 of 20

Frequently asked questions

How many devices does Life Science Instrumentation, Inc. have in the registry?

The registry currently lists 20 devices for Life Science Instrumentation, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Life Science Instrumentation, Inc.'s devices?

Among its 20 most recently registered devices, Life Science Instrumentation, Inc. has devices listed in FDA 510(k) (20 devices).

What risk classes do Life Science Instrumentation, Inc.'s devices fall under?

Among its 20 most recently registered devices, the classes recorded for Life Science Instrumentation, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Life Science Instrumentation, Inc. in the registry?

The most recently registered devices listed for Life Science Instrumentation, Inc. include LS-260G MONITOR/RECORDER & DEFIBILLATOR, PIONEER II BACK PLATE ELECTRODE, MINI-DEFIBRILLATOR 280/4 and CARDIORATER CR-3.

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