mo-vis BV
Active in EUDAMEDBelgiumfrom SRN EUDAMED FDA SRN BE-MF-000000729 FEI 3011795161
mo-vis BV is a medical device manufacturer based in Belgium, with 110 devices listed in EUDAMED and FDA GUDID (EU Class I) and 7 FDA recalls as of 15 Nov 2026.
- Devices
- 110
- Registrations
- EUDAMEDFDA
- FDA recalls
- 77 ongoing
Registry facts
- Registries
- EUDAMED 110
- FDA GUDID 109
- Device classes
- EU Class I 110
- Top EMDN categories
- FDA recalls
- Identifiers
- EUDAMED SRN BE-MF-000000729
- FDA FEI 3011795161
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA establishment, FDA recalls
Catalogue
Search and filter all 110 devicesShowing 1-50 of 110
Company details
- EUDAMED SRN
- BE-MF-000000729
- FDA FEI number
- 3011795161
- EU VAT number
- BE0540663251
- EUDAMED status
- Active
- EUDAMED registered name
- mo-vis bv
- Registered address
- 15D, Biebuyckstraat, 9850, Deinze, Belgium
- Website
- www.mo-vis.com
- Phone
- +3293352860
- PRRC contact
- Marcel Frère
FDA recalls
Recalls initiated per year
- 2017 0
- 2018 0
- 2019 0
- 2020 0
- 2021 0
- 2022 0
- 2023 1
- 2024 0
- 2025 6
- 2026 0
2025
- 10 Jul 2025 Z-2454-2025 Class I Ongoing Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
- 10 Jul 2025 Z-2455-2025 Class I Ongoing Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
- 10 Jul 2025 Z-2456-2025 Class I Ongoing Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
- 10 Jul 2025 Z-2457-2025 Class I Ongoing Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
- 10 Jul 2025 Z-2458-2025 Class I Ongoing Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
- 10 Jul 2025 Z-2459-2025 Class I Ongoing Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
2023
- 28 Nov 2023 Z-0713-2024 Class II Ongoing In rare cases, the lever of the throttle can get temporarily stuck during the movement and does not come back to its neutral point by itself. If this happens during usage, an unwanted movement of the chair could be the result. An unwanted movement could result in damage to the wheelchair, material damage around the chair and/or injury to the user, attendant or by-standers.
FDA establishments
- mo-Vis US
Frequently asked questions
How many devices does mo-vis bv have in the registry?
The registry currently lists 110 devices for mo-vis bv. Devices recorded under merged duplicate company entries are counted once.
Which registries list mo-vis bv's devices?
Among its 50 most recently registered devices, mo-vis bv has devices listed in EUDAMED (50 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do mo-vis bv's devices fall under?
Among its 50 most recently registered devices, the classes recorded for mo-vis bv's devices are Class I. Each device page shows its own class and authorisation.
Are there FDA recall records for mo-vis bv?
FDA recall records list 7 recalls initiated by mo-vis bv, the most recent initiated on 10 Jul 2025. 7 of them are recorded as ongoing. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from mo-vis bv in the registry?
The most recently registered devices listed for mo-vis bv include Function Keypad Button LiNX, Function Keypad Paddle LiNX, Twister Pro (D36) Red Q2M Set and Twister Basic, (300mm), Green.
Which FDA establishments are linked to mo-vis bv?
1 FDA establishment is linked to mo-vis bv in the registry; they are listed on the company page.