Data / Medical devices / Stimulator, Electrical, Non-Implantable, For Incontinence / China
FDA-registered makers of Stimulator, Electrical, Non-Implantable, For Incontinence in China: 7 establishments
7 establishments in China are registered with the FDA to make Stimulator, Electrical, Non-Implantable, For Incontinence (product code KPI). 6 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
- Stimulator, Electrical, Non-Implantable, For Incontinence
- Product code
- KPI
- Country
- China
Makers of Stimulator, Electrical, Non-Implantable, For Incontinence in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Shenzhen Konmed Technology Co., Ltd | Shenzhen Guangdong, China | Complaint file establishment, Manufacturer, Repackager or relabeler | 4 | June 18, 2026 | 0 | 0 | 0 | api.fda.gov |
| Dolanvy (Suzhou) Medical Technology Co., Ltd | Suzhou Jiangsu, China | Manufacturer | 1 | April 28, 2026 | 0 | 0 | 0 | api.fda.gov |
| Easymed Instruments Co., Ltd. | Daliang, Shunde, Foshan Guangdong, China | Manufacturer | 1 | November 27, 2024 | 0 | 0 | 0 | api.fda.gov |
| Netop Industrial Company Limited | Dongguan Guangdong, China | Manufacturer | 1 | April 13, 2022 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Changkun Technology Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 1 | May 6, 2026 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Med-Link Electronics Tech Co.,ltd | Shenzhen Guangdong, China | Manufacturer | 1 | September 17, 2021 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Dongdixin Technology Co., Ltd. | SHENZHEN 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.