Skip to content

Cole & Associates

Country not established

Devices
1

What Cole & Associates makes

Cole & Associates manufactures the MENTAMOVE, a device designed for cognitive or behavioral therapy applications, likely targeting conditions such as ADHD or related disorders.

The MENTAMOVE is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Mentamove Ref K040849

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

Frequently asked questions

How many devices does Cole & Associates have in the registry?

The registry currently lists 1 device for Cole & Associates. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cole & Associates's devices?

Among its 1 most recently registered device, Cole & Associates has devices listed in FDA 510(k) (1 device).

What risk classes do Cole & Associates's devices fall under?

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

What are the newest devices from Cole & Associates in the registry?

The most recently registered devices listed for Cole & Associates include MENTAMOVE.

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