Data / Medical devices / Sleeve, Limb, Compressible / China
FDA-registered makers of Sleeve, Limb, Compressible in China: 23 establishments
23 establishments in China are registered with the FDA to make Sleeve, Limb, Compressible (product code JOW). 14 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Sleeve, Limb, Compressible
- Product code
- JOW
- Country
- China
Makers of Sleeve, Limb, Compressible in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Devon Medical Products (jiangsu) Ltd | Nantong Jiangsu, China | Manufacturer | 6 | March 19, 2019 | 0 | 0 | 0 | api.fda.gov |
| MedHealth Medical Limited | Shenzhen Guangdong, China | Contract manufacturer, Manufacturer | 5 | December 14, 2023 | 0 | 0 | 0 | api.fda.gov |
| Arjo (Suzhou) Co., Ltd. | Suzhou Jiangsu, China | Contract manufacturer, Manufacturer, Specification developer | 3 | June 23, 2015 | 0 | 0 | 0 | api.fda.gov |
| Dalian Labtek Science & Development Co Ltd | Dalian Liaoning, China | Exporter to the US, Manufacturer | 3 | February 9, 2022 | 0 | 0 | 0 | api.fda.gov |
| JKH Health Co., Ltd. | Dongguan Guangdong, China | Contract manufacturer, Manufacturer | 3 | February 23, 2024 | 0 | 0 | 0 | api.fda.gov |
| Jiangsu Synecoun Medical Technology Co., Ltd. | Taizhou City Jiangsu, China | Manufacturer | 2 | November 18, 2021 | 0 | 0 | 0 | api.fda.gov |
| Suzhou Minhua Medical Equipment Co.,Ltd. | SuZhou Jiangsu, China | Complaint file establishment, Contract manufacturer, Exporter to the US, Manufacturer | 2 | January 15, 2025 | 0 | 0 | 0 | api.fda.gov |
| Alleva Medical (D.G.) Ltd | Dongguan City Guangdong, China | Contract manufacturer, Manufacturer | 1 | August 27, 2019 | 0 | 0 | 0 | api.fda.gov |
| Apex Medical (Kunshan) Corp. | Kunshan City Jiangsu, China | Manufacturer | 1 | October 28, 2025 | 0 | 0 | 0 | api.fda.gov |
| Guangzhou Longest Medical Technology Co., Ltd. | Guangzhou Guangdong, China | Manufacturer | 1 | April 24, 2026 | 0 | 0 | 0 | api.fda.gov |
| Huaian Youwen Medical Technology Co.,ltd | HUAIAN Jiangsu, China | Manufacturer | 1 | November 9, 2011 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Xinrun Electric Appliances Co Ltd | Shenzhen Guangdong, China | Contract manufacturer, Manufacturer | 1 | February 22, 2013 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Pango Medical Electronics Co., Ltd | Shenzhen Guangdong, China | Manufacturer | 1 | November 10, 2021 | 0 | 0 | 0 | api.fda.gov |
| Vistar Medical Supplies Co., Ltd. | SHENZHEN Guangdong, China | Manufacturer | 1 | June 25, 2026 | 0 | 0 | 0 | api.fda.gov |
| Dongguan Esino Manufacturing Service Co., Ltd | Dongguan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Foshan Hongfeng Co.,ltd | Foshan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Grandway Technology (shenzhen) Limited | Shenzhen Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangsu Reak Healthy Articles Co.,ltd | Yangzhong City Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiaxing Max Hosiery Co.,Ltd. | Jiaxing Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ningbo Albert Novosino Co., Ltd. | Yuyao Zhejiang, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Homed Medical Device Co Ltd | Dongguan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai Caremate Medical Device Co. Ltd | Shanghai, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Xiamen Weiyou Intelligent Technology Co.,Ltd | xiamen Fujian, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.