Hoveround Corp.
United StatesFDA applicant, unverified
Hoveround Corp. is a medical device manufacturer, with 23 devices listed in FDA 510(k) and FDA GUDID (FDA Class II) as of 15 Nov 2026.
- Devices
- 23
Registry facts
- Registries
- FDA 510(k) 17
- FDA GUDID 6
- Device classes
- FDA Class II 23
What Hoveround Corp. makes
Hoveround Corp. manufactures electric-motor-driven, occupant-controlled, powered-steering, non-collapsible wheelchairs. These include models such as the Hoveround, Teknique-Hoveround Power Wheel Chair, Hoveround Power Wheelchair or HVR-200, Teknique Model HD-6, SE-3 Powerchair, Teknique, and Hoverglide Model Hoverglide MK-2.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries.
Catalogue
Search and filter all 23 devicesFrequently asked questions
How many devices does Hoveround Corp. have in the registry?
The registry currently lists 23 devices for Hoveround Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hoveround Corp.'s devices?
Among its 23 most recently registered devices, Hoveround Corp. has devices listed in FDA 510(k) (17 devices) and FDA GUDID (6 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Hoveround Corp.'s devices fall under?
Among its 23 most recently registered devices, the classes recorded for Hoveround Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hoveround Corp. in the registry?
The most recently registered devices listed for Hoveround Corp. include Hoveround LX-5, Hoveround Teknique HD-6, Hoveround Teknique XHD and Hoveround Teknique FWD.