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Biofax Medical Instrumentation Co.

Country not established

Devices
1

What Biofax Medical Instrumentation Co. makes

Biofax Medical Instrumentation Co. manufactures blood flow analyzers designed to measure and assess circulatory dynamics in clinical settings. These devices are intended for use in diagnostic evaluations to support cardiovascular assessments.

The company’s portfolio is regulated under Class II devices in the US and is listed via FDA 510(k) clearance. The devices are based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Blood Flow Analyzer Ref K820959

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

Frequently asked questions

How many devices does Biofax Medical Instrumentation Co. have in the registry?

The registry currently lists 1 device for Biofax Medical Instrumentation Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Biofax Medical Instrumentation Co.'s devices?

Among its 1 most recently registered device, Biofax Medical Instrumentation Co. has devices listed in FDA 510(k) (1 device).

What risk classes do Biofax Medical Instrumentation Co.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Biofax Medical Instrumentation Co.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Biofax Medical Instrumentation Co. in the registry?

The most recently registered devices listed for Biofax Medical Instrumentation Co. include BLOOD FLOW ANALYZER.

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