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Zenyx Scientific, Ltd.

United KingdomFDA 510(k) applicant, unverified

Devices
1

What Zenyx Scientific, Ltd. makes

Zenyx Scientific, Ltd. manufactures the QUATRO SP Sample Processing Systems, designed for automated sample preparation in laboratory settings, handling volumes between 200 and 499 units.

The company’s portfolio is regulated under Class I medical devices in the U.S. and is listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

Frequently asked questions

How many devices does Zenyx Scientific, Ltd. have in the registry?

The registry currently lists 1 device for Zenyx Scientific, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Zenyx Scientific, Ltd.'s devices?

Among its 1 most recently registered device, Zenyx Scientific, Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Zenyx Scientific, Ltd.'s devices fall under?

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

What are the newest devices from Zenyx Scientific, Ltd. in the registry?

The most recently registered devices listed for Zenyx Scientific, Ltd. include QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE).

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