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Health America

Country not established

Devices
1

What Health America makes

Health America manufactures a range of wheelchair models designed for mobility assistance, including manual and potentially motorised variants for diverse patient needs.

These devices fall under Class I regulatory classification in the US, with individual models authorised via FDA 510(k) clearance. 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

  • Wheelchair-Various Models Ref K832685

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

Frequently asked questions

How many devices does Health America have in the registry?

The registry currently lists 1 device for Health America. Devices recorded under merged duplicate company entries are counted once.

Which registries list Health America's devices?

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

What risk classes do Health America's devices fall under?

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

What are the newest devices from Health America in the registry?

The most recently registered devices listed for Health America include WHEELCHAIR-VARIOUS MODELS.

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