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Vipamat Technologie

Country not established

Devices
1

What Vipamat Technologie makes

Vipamat Technologie manufactures the Hippocampe wheelchair, a mobility aid designed for users requiring specialized seating and positioning support.

The company’s products are regulated as Class II medical devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The manufacturer 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

  • Hippocampe Wheelchair Ref K051709

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

Frequently asked questions

How many devices does Vipamat Technologie have in the registry?

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

Which registries list Vipamat Technologie's devices?

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

What risk classes do Vipamat Technologie's devices fall under?

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

What are the newest devices from Vipamat Technologie in the registry?

The most recently registered devices listed for Vipamat Technologie include HIPPOCAMPE WHEELCHAIR.

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