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Creative Design Systems, Inc.

Country not established

Devices
1

What Creative Design Systems, Inc. makes

Creative Design Systems, Inc. manufactures transcutaneous electrical nerve stimulation (TENS) conductive media pads, designed for pain management applications.

These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records in the U.S. The company is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Tens Conductive Media Pad Ref K904889

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

Frequently asked questions

How many devices does Creative Design Systems, Inc. have in the registry?

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

Which registries list Creative Design Systems, Inc.'s devices?

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

What risk classes do Creative Design Systems, Inc.'s devices fall under?

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

What are the newest devices from Creative Design Systems, Inc. in the registry?

The most recently registered devices listed for Creative Design Systems, Inc. include TENS CONDUCTIVE MEDIA PAD.

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