Data / Medical devices / Cuff, Pusher, Wheelchair / China
FDA-registered makers of Cuff, Pusher, Wheelchair in China: 11 establishments
11 establishments in China are registered with the FDA to make Cuff, Pusher, Wheelchair (product code INC). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Cuff, Pusher, Wheelchair
- Product code
- INC
- Country
- China
Makers of Cuff, Pusher, Wheelchair in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| China Wonderland Nurserygoods Co., Ltd. | Dongguan City Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Chiaphua Components (Jiangxi) Limited | Yichun city Jiangxi, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Feishen Group CO., LTD. | yongkang Zhejiang, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Global Fabtech Wheel Chair (shanghai) Co., Ltd. | Shanghai, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangdong Hexin Technology Weaving Co., LTD | Huizhou City Guangdong, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangdong Marshell Electric Vehicle CO., LTD. | Zhaoqing Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kunshan Hi-Fortune Health Products Co., Ltd. | Kunshan City, Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Merits Healthcare Industries. (suzhou) Co., Ltd. | Jiangsu Province, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Permobil (kunshan) Co., Ltd | Kunshan Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Trolli King (holding) Ltd. | Shenzhen Guangdong, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Viscount Hi-Tech (huizhou) Co., Ltd. | Huizhou Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.