Data / Medical devices / Epilator, High Frequency, Tweezer-Type / China
FDA-registered makers of Epilator, High Frequency, Tweezer-Type in China: 10 establishments
10 establishments in China are registered with the FDA to make Epilator, High Frequency, Tweezer-Type (product code KCX). 0 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
- Epilator, High Frequency, Tweezer-Type
- Product code
- KCX
- Country
- China
Makers of Epilator, High Frequency, Tweezer-Type in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Dongguan Yibiao Electronic Technology Co.,ltd | Dong Guan City Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DayOn Daily Chemical Co., Ltd | Yangzhou Jiangsu, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ever Strong Manufacturing Ltd | Dongguan Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Foshan CICADA Dental Instrument Co., Ltd. | Foshan Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangdong Comfort Medical Products Co., Ltd. | Jiangmen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lianyungang Brilliant Industrial Co., Ltd. | LIANYUNGANG Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Eyco Technology Co.,ltd | Shenzhen Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Rogin Medical Co., Ltd | shenzhen Guangdong, China | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Yuhuan City Shengbo Mould Manufacturing Co.,Ltd. | Yuhuan Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zhongshan Kingdom Electrical Appliance Co., Ltd. | Zhongshan Guangdong, China | Exporter to the US, 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.