Mo-Vis

Micro Joystick Omni Permobil set (PRSPS00020)

Registry build 21.09.26
54manufacturers in China registered for this device type
123catalogue numbers in this listing
7recalls on this code

Who Else Makes It

Concentrated in Jiangsu (18), Guangdong (14), Zhejiang (11). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KNN
Manufacturer City Province Registered as Device types
Kunshan Hi-Fortune Health Products Co., Ltd. Kunshan Jiangsu Contract manufacturer 32
Chiaphua Components (Jiangxi) Limited Yichun Jiangxi Contract manufacturer 23
Feishen Group Co., Ltd. Yongkang Zhejiang Contract manufacturer 22
Guangdong Marshell Electric Vehicle Co., Ltd. Zhaoqing Guangdong Contract manufacturer 22
Jiangyin Huashi Medical Equipment Co., Ltd. Jiangyin Jiangsu Contract manufacturer 21
Zhenjiang Assure Medical Equipment Co Ltd Zhenjiang Jiangsu Contract manufacturer 18
Jiangsu Yuyue Medical Equipment & Supply Company Limited Jiangsu Jiangsu Contract manufacturer 17
Raise Medical Industries, Inc. Foshan Guangdong Contract manufacturer 16
Permobil Trading (Kunshan) Co., Ltd. Kunshan Jiangsu Contract manufacturer 8
Three Bears (Jiangsu) Healthcare Technology Co., Ltd. Changzhou Jiangsu Contract manufacturer 6
Irest Health Science AND Technology Co., Ltd. Jiaxing Zhejiang Contract manufacturer 5
Zhejiang Linix Motor Co., Ltd. Dongyang Zhejiang Contract manufacturer 4

Showing 12 of 54. All 54 manufacturers in China registered for Components, Wheelchair

Record

Regulatory record for mo-Vis
Listed by MO-VIS BV, Belgium
FDA product code KNN
Device type Components, Wheelchair
Device class Class 1
Regulation 21 CFR 890.3920
Establishment Manufacturer
Premarket notification Exempt
Record published 2020-08-31
Record revised 2025-11-20 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Supplied as a kit Yes
Label carries lot or batch number, manufacturing date, serial number
Distribution end date 2022-11-23

Catalogue Numbers

Catalogue numbers for mo-Vis
Catalogue number Size Status
P005-60 In distribution
P032-52 Sip and Puf Module In distribution
P005-64 In distribution
P002-62 In distribution
P030-21 In distribution
P015-61 In distribution
P030-13 In distribution
P005-43 In distribution
P010-61 In distribution
P021-53 In distribution
P032-51 In distribution
P001-23 In distribution
P002-54 In distribution
P005-63 In distribution
IDM-MULTI-9 In distribution
P002-72 In distribution
P016-96 In distribution
P002-75 In distribution
P005-19 In distribution
P005-74 In distribution
IDM-ALLROUND-R In distribution
P005-15 In distribution
P015-76 In distribution
P030-31 In distribution
P030-12 In distribution
P018-20 In distribution
P005-42 In distribution
P001-60 In distribution
M013-61 In distribution
P015-77 In distribution
P015-86 In distribution
P031-21 In distribution
P005-71 In distribution
P005-87 In distribution
P018-24 In distribution
P016-89 In distribution
P016-86 In distribution
P005-44 In distribution
P002-64 In distribution
P018-22 In distribution
P005-86 In distribution
P016-88 In distribution
P016-87 In distribution
P002-71 In distribution
P018-21 In distribution
P015-85 In distribution
P005-73 In distribution
P010-52 In distribution
P005-79 In distribution
P005-17 In distribution
P015-81 In distribution
P005-75 In distribution
P031-50 In distribution
P005-89 In distribution
P002-73 In distribution
P002-55 In distribution
P005-54 In distribution
P001-63 In distribution
P001-21 In distribution
P031-22 In distribution
P005-70 In distribution
Micro Joystick Omni Permobil set In distribution
P002-61 In distribution
P030-11 In distribution
P005-51 In distribution
P030-43 In distribution
P014-40 In distribution
IDM-MULTI-R In distribution
P001-50 In distribution
P030-41 In distribution
P030-33 In distribution
P005-62 In distribution
P005-61 In distribution
P031-61 In distribution
P031-62 In distribution
P005-88 In distribution
P001-24 In distribution
P021-51 In distribution
P031-63 In distribution
P005-18 In distribution
P005-77 In distribution
P015-71 In distribution
P005-52 In distribution
P005-72 In distribution
P002-76 In distribution
P030-32 In distribution
P030-22 In distribution
P001-61 In distribution
P011-61 Head Control Omni Proportional In distribution
P018-23 In distribution
P016-99 In distribution
IDM-ALLROUND-9 In distribution
P015-66 In distribution
IDM-ARLITE-9 In distribution
P005-78 In distribution
P005-16 In distribution
P002-52 In distribution
P016-97 In distribution
P021-52 In distribution
IDM-MICRO-9 In distribution
P034-71 R-net Switch Control In distribution
P001-62 In distribution
P005-76 In distribution
P005-40 In distribution
P030-42 In distribution
P011-62 Head Control Omni Switched In distribution
IDM-MS In distribution
P016-98 In distribution
P005-53 In distribution
P005-41 In distribution
IDM-MICRO-R In distribution
P015-65 In distribution
P011-63 Head Control Omni Proportional Short In distribution
P030-23 In distribution
P012-62 In distribution
IDM-ARLITE-R In distribution
P002-51 In distribution
Multi Joystick Omni Permobil set In distribution
P005-50 In distribution
P001-22 In distribution
P002-77 In distribution
P005-85 In distribution
P031-23 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Action® Action Products, Inc. 233
Axiom Ki Mobility 182
Spex Limited Spex Ltd 132
Medline Medline Industries, Inc. 111
Everest & Jennings GF Health Products, Inc 108
Spex Spex Ltd 70
Drive Drive DeVilbiss Healthcare 36
Evermed Xiamen Taft Medical Co., Ltd. 30
Drivemedical Drive DeVilbiss Healthcare 24
Cardinal Health Cardinal Health 200, LLC 23
CoMoveIT Comoveit 8
Spex Seating Spex Ltd 7

Showing 12 of 159. All products under Components, Wheelchair

Recalls Naming This Product

7 recalls name this product by its own identifiers, the UDI on its label.

Recalls naming the identifiers of mo-Vis
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
MO-VIS BV UDI-DI 2025-07-10 Class I Device Design 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 joystic 3 units
MO-VIS BV UDI-DI 2025-07-10 Class I Device Design 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 joystic 3 units
MO-VIS BV UDI-DI 2025-07-10 Class I Device Design 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 joystic 15 units
MO-VIS BV UDI-DI 2025-07-10 Class I Device Design 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 joystic 15 units
MO-VIS BV UDI-DI 2025-07-10 Class I Device Design 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 joystic 3 units
MO-VIS BV UDI-DI 2025-07-10 Class I Device Design 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 joystic 25 units
MO-VIS BV UDI-DI 2023-11-28 Class II Device Design 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 m 129 units

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer