Data / Medical devices / Stimulator, Transcutaneous Electrical, Aesthetic Purposes / China
FDA-registered makers of Stimulator, Transcutaneous Electrical, Aesthetic Purposes in China: 22 establishments
22 establishments in China are registered with the FDA to make Stimulator, Transcutaneous Electrical, Aesthetic Purposes (product code NFO). 14 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, Transcutaneous Electrical, Aesthetic Purposes
- Product code
- NFO
- Country
- China
Makers of Stimulator, Transcutaneous Electrical, Aesthetic Purposes in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Shenzhen Siken 3D Technology Development Co., Ltd. | Dongguan Guangdong, China | Manufacturer | 2 | December 23, 2025 | 0 | 0 | 0 | api.fda.gov |
| Vis (shanghai) Technology Co., Ltd. | Jinshan District Shanghai, China | Manufacturer | 2 | May 13, 2024 | 0 | 0 | 0 | api.fda.gov |
| Ever Strong Manufacturing Ltd | Dongguan Guangdong, China | Manufacturer | 1 | December 9, 2011 | 0 | 0 | 0 | api.fda.gov |
| Guangdong Newdermo Biotech Co., Ltd | Guangzhou Guangdong, China | Manufacturer | 1 | September 16, 2026 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Aozemei Technology Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 1 | December 19, 2024 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Dachi Communication Co.,ltd. | Shenzhen Guangdong, China | Manufacturer | 1 | July 10, 2025 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Jianchao Intelligent Technology Co., Ltd. | Shenzhen Guangdong, China | Foreign private label distributor, Manufacturer | 1 | October 9, 2025 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Kizoku Life Technology Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 1 | November 24, 2023 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Nuon Medical Equipment Co., Ltd. | ShenZhen Guangdong, China | Manufacturer | 1 | October 12, 2025 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Qianyu Technology Co., Ltd. | Shenzhen Guangdong, China | Specification developer | 1 | October 17, 2025 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Ulike Smart Electronics Co.,ltd | Shenzhen Guangdong, China | Manufacturer | 1 | February 3, 2025 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Kaiyan Medical Equipment Co., Ltd | Shenzhen Guangdong, China | Exporter to the US, Manufacturer | 1 | July 23, 2026 | 0 | 0 | 0 | api.fda.gov |
| Touchbeauty Beauty & Health (shenzhen) Co., Ltd | Shenzhen Guangdong, China | Manufacturer | 1 | June 3, 2026 | 0 | 0 | 0 | api.fda.gov |
| Zhongshan Kingdom Electrical Appliance Co., Ltd. | Zhongshan Guangdong, China | Exporter to the US, Manufacturer | 1 | April 26, 2018 | 0 | 0 | 0 | api.fda.gov |
| Foshan Shiding Technology Co., Ltd. | Foshan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangdong Ace-Tec Co., Ltd. | Dongguan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hong Qiangxing (shen Zhen) Electronics Limited | Shenzhen Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rosti Integrated Manufacturing Solutions (suzhou) Co., Ltd. | Suzhou Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Huayan E-Commerce Co., Ltd. | Shenzhen Guangdong, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Xiangzhida Technology Co.,ltd. | Shenzhen Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Zowee Smart Manufacturing Co., Ltd. | Shenzhen Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Xiamen Solex High-Tech Industries Co.,ltd | Xiamen Fujian, China | Contract 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.