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Briar Cliff, Inc.

Country not established

Devices
1

What Briar Cliff, Inc. makes

Briar Cliff, Inc. manufactures the ACCU.CROWN COLD CURE, a device designed for cold therapy applications, likely intended for pain management or post-procedural recovery.

The device falls under FDA Class II regulation and is listed via 510(k) clearance. 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

  • Accu. Crown Cold Cure Ref K771254

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

Frequently asked questions

How many devices does Briar Cliff, Inc. have in the registry?

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

Which registries list Briar Cliff, Inc.'s devices?

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

What risk classes do Briar Cliff, Inc.'s devices fall under?

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

What are the newest devices from Briar Cliff, Inc. in the registry?

The most recently registered devices listed for Briar Cliff, Inc. include ACCU. CROWN COLD CURE.

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