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Stoneheart, Inc.

Country not established

Devices
1

What Stoneheart, Inc. makes

Stoneheart, Inc. manufactures the Stoneheart Roller Aid, a mobility assistance device designed to aid users in transferring or repositioning while seated or lying down.

The company’s product portfolio is regulated under Class I medical devices in the US and is listed in the FDA’s 510(k) clearance registry. Stoneheart, Inc. 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

  • Stoneheart Roller Aid Ref K925247

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

Frequently asked questions

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

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

Which registries list Stoneheart, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Stoneheart, Inc. include STONEHEART ROLLER AID.

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