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Dedo Manufacturer, Inc.

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Devices
1

What Dedo Manufacturer, Inc. makes

Dedo Manufacturer, Inc. produces the DEDO Suction Cannula, a Class I medical device designed for aspiration applications in clinical settings.

The device is regulated under the FDA’s 510(k) pathway and is listed in the U.S. regulatory database. The company 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

  • Dedo Suction Cannula Ref K854005

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

Frequently asked questions

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

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

Which registries list Dedo Manufacturer, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Dedo Manufacturer, Inc. include DEDO SUCTION CANNULA.

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