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Accor, Inc.

Country not established

Devices
1

What Accor, Inc. makes

Accor, Inc. manufactures the ACCOR MATRIX device, which is categorized under Class I medical devices.

The company is based in the US and its devices are listed in the FDA 510(k) registry.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Accor Matrix Ref K790633

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

Frequently asked questions

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

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

Which registries list Accor, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Accor, Inc. include ACCOR MATRIX.

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