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Quadroma, Inc.

Country not established

Devices
1

What Quadroma, Inc. makes

Quadroma, Inc. manufactures coagulase plasma, a reagent used in microbiological testing to identify bacterial species capable of producing coagulase enzymes.

The coagulase plasma is classified as a Class I medical device under FDA regulations and is 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

  • Coagulase Plasma Ref K820177

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

Frequently asked questions

How many devices does Quadroma, Inc. have in the registry?

The registry currently lists 1 device for Quadroma, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Quadroma, Inc.'s devices?

Among its 1 most recently registered device, Quadroma, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Quadroma, Inc.'s devices fall under?

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

What are the newest devices from Quadroma, Inc. in the registry?

The most recently registered devices listed for Quadroma, Inc. include COAGULASE PLASMA.

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