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Life Sciences Manufacturing, Inc.

United StatesFDA applicant, unverified

Devices
12

What Life Sciences Manufacturing, Inc. makes

Life Sciences Manufacturing, Inc. produces diagnostic and monitoring devices for vascular and cardiovascular assessments, including non-invasive clinical vascular labs, microprocessor-controlled modules for pressure and volume measurements, and automated physiologic profile monitors. Their portfolio includes specialized modules for arterial-venous recording, cutaneous pressure plethysmography, and portable air plethysmography, as well as systems for pulse volume recording and photoplethysmography.

The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory clearance obtained through the 510(k) pathway. These products are listed in the FDA’s 510(k) database, reflecting their compliance with 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.

Catalogue12

Newest first, rows 1-12 of 12

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  • Non-Invasive Clinical Vascular Lab Ref K832679

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

  • Sfa-Ii Microprocessor-Controlled Module Ref K910905

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

  • Sfa Module Ref K896528

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

  • A-V Recorder Ref K873041

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

  • Mvl/Modulab With Pvr Module Ref K884624

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

  • Pag Microprocessor-Controlled Module Ref K900365

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

  • Vdc Ref K791756

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

  • Cutaneous Pressure Plethysmograph Ref K822522

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

  • Cwd/Ppg Module Ref K896500

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

  • Ipg-Ii Module Ref K903700

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

  • Portable Air Plethysmograph Ref K895588

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

  • Automated Physiologic Profile Monitor Ref K811560

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

Rows 1-12 of 12

Frequently asked questions

How many devices does Life Sciences Manufacturing, Inc. have in the registry?

The registry currently lists 12 devices for Life Sciences Manufacturing, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Life Sciences Manufacturing, Inc.'s devices?

Among its 12 most recently registered devices, Life Sciences Manufacturing, Inc. has devices listed in FDA 510(k) (12 devices).

What risk classes do Life Sciences Manufacturing, Inc.'s devices fall under?

Among its 12 most recently registered devices, the classes recorded for Life Sciences Manufacturing, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Life Sciences Manufacturing, Inc. in the registry?

The most recently registered devices listed for Life Sciences Manufacturing, Inc. include NON-INVASIVE CLINICAL VASCULAR LAB, SFA-II MICROPROCESSOR-CONTROLLED MODULE, SFA MODULE and A-V RECORDER.

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