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Dia-Stron, Ltd.

Country not established

Devices
1

What Dia-Stron, Ltd. makes

Dia-Stron, Ltd. manufactures the Oxford Optronix MPM 3S, a medical imaging device designed for monitoring and analyzing patient movement and posture, particularly in clinical or research settings.

The company’s portfolio is regulated under FDA’s Class II device classification and is listed in the 510(k) premarket notification process. 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

  • Oxford Optronix Mpm 3S Ref K914397

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

Frequently asked questions

How many devices does Dia-Stron, Ltd. have in the registry?

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

Which registries list Dia-Stron, Ltd.'s devices?

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

What risk classes do Dia-Stron, Ltd.'s devices fall under?

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

What are the newest devices from Dia-Stron, Ltd. in the registry?

The most recently registered devices listed for Dia-Stron, Ltd. include OXFORD OPTRONIX MPM 3S.

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