mo-Vis
Country not established
Part of mo-vis BV
mo-Vis is a medical device manufacturer, with 19 devices listed in FDA GUDID and EUDAMED (FDA Class I) as of 15 Nov 2026.
- Devices
- 19
Registry facts
- Registries
- FDA GUDID 19
- EUDAMED 3
- Device classes
- FDA Class I 19
- Sites and related companies
- Identifiers
- DUNS 370456732
What mo-Vis makes
mo-Vis designs assistive positioning systems that enable rotating and sliding adjustments for users, along with input-control training devices focused on selection techniques for improved accessibility. Their portfolio also includes wheelchair steering and control units, as well as variable-voltage power supplies tailored for assistive mobility solutions.
All mo-Vis devices fall under FDA Class I regulation and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States.
Catalogue
Search and filter all 19 devicesCompany details
- DUNS number
- 370456732
Frequently asked questions
How many devices does mo-Vis have in the registry?
The registry currently lists 19 devices for mo-Vis. Devices recorded under merged duplicate company entries are counted once.
Which registries list mo-Vis's devices?
Among its 19 most recently registered devices, mo-Vis has devices listed in EUDAMED (3 devices) and FDA GUDID (19 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do mo-Vis's devices fall under?
Among its 19 most recently registered devices, the classes recorded for mo-Vis's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from mo-Vis in the registry?
The most recently registered devices listed for mo-Vis include mo-vis P002-78 All-round Joystick LiNX, mo-vis P002-79 All-round Joystick LiNX Light, mo-vis and mo-Vis P031-23.