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Coolanalgesia, Ltd.

United KingdomFDA applicant, unverified

Devices
1

What Coolanalgesia, Ltd. makes

Coolanalgesia, Ltd. manufactures the COOLAN 300, a device designed for localized cooling therapy, likely used in pain management or post-procedural care.

The COOLAN 300 is classified as a Class II medical device and is listed under the FDA’s 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

  • Coolan 300 Ref K030810

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

Frequently asked questions

How many devices does Coolanalgesia, Ltd. have in the registry?

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

Which registries list Coolanalgesia, Ltd.'s devices?

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

What risk classes do Coolanalgesia, Ltd.'s devices fall under?

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

What are the newest devices from Coolanalgesia, Ltd. in the registry?

The most recently registered devices listed for Coolanalgesia, Ltd. include COOLAN 300.

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