Skip to content

Custom Industries, Inc.

Country not established

Devices
1

What Custom Industries, Inc. makes

Custom Industries, Inc. manufactures the ULTRAFLOW, a medical device designed for controlled fluid delivery in clinical settings.

The ULTRAFLOW is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. 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

  • Ultraflow Ref K871901

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

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

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

Which registries list Custom Industries, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Custom Industries, Inc. include ULTRAFLOW.

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