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Soredex, Inc.

FinlandFDA applicant, unverified

Devices
1

What Soredex, Inc. makes

Soredex, Inc. manufactures dental chair units, specifically the MAMEX DC AMI SL12/MG15 model, designed for dental procedures and patient comfort.

The company’s portfolio is regulated under Class II medical devices in the United States, with the MAMEX DC AMI SL12/MG15 listed via a 510(k) clearance. The company is based in the US.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Mamex Dc Ami SL12/MG15 Ref K905748

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

Frequently asked questions

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

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

Which registries list Soredex, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Soredex, Inc. include MAMEX DC AMI SL12/MG15.

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