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Marshall Levinson

Country not established

Devices
1

What Marshall Levinson makes

Marshall Levinson makes the DIFF SAFE device.

The DIFF SAFE device is classified as Class II and is listed in the FDA 510(k) registry. 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

  • Diff Safe Ref K914129

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

Frequently asked questions

How many devices does Marshall Levinson have in the registry?

The registry currently lists 1 device for Marshall Levinson. Devices recorded under merged duplicate company entries are counted once.

Which registries list Marshall Levinson's devices?

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

What risk classes do Marshall Levinson's devices fall under?

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

What are the newest devices from Marshall Levinson in the registry?

The most recently registered devices listed for Marshall Levinson include DIFF SAFE.

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