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Dia-Screen Corp.

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Devices
1

What Dia-Screen Corp. makes

Dia-Screen Corp. manufactures reagent strips for diagnostic testing, designed for use in detecting substances such as glucose, ketones, or protein in bodily fluids like urine.

These products fall under FDA Class I devices and are listed via the 510(k) pathway. The company is 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

  • Diascreen Reagent Strips Ref K971976

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

Frequently asked questions

How many devices does Dia-Screen Corp. have in the registry?

The registry currently lists 1 device for Dia-Screen Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dia-Screen Corp.'s devices?

Among its 1 most recently registered device, Dia-Screen Corp. has devices listed in FDA 510(k) (1 device).

What risk classes do Dia-Screen Corp.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Dia-Screen Corp.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Dia-Screen Corp. in the registry?

The most recently registered devices listed for Dia-Screen Corp. include DIASCREEN REAGENT STRIPS.

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