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Normandie Group, Inc.

Country not established

Devices
1

What Normandie Group, Inc. makes

Normandie Group, Inc. manufactures the FMA Translator, a device designed for translating medical imaging data formats, ensuring compatibility between different systems and modalities.

The FMA Translator is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Fma Translator Ref K912086

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

Frequently asked questions

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

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

Which registries list Normandie Group, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Normandie Group, Inc. include FMA TRANSLATOR.

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