Data / Medical devices / Powered Microneedle Device / China
FDA-registered makers of Powered Microneedle Device in China: 8 establishments
8 establishments in China are registered with the FDA to make Powered Microneedle Device (product code QAI). 2 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
- Powered Microneedle Device
- Product code
- QAI
- Country
- China
Makers of Powered Microneedle Device in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Guangdong Carain Beauty Equipment Co., Ltd | Foshan Guangdong, China | Contract manufacturer, Manufacturer | 4 | October 29, 2025 | 0 | 0 | 0 | api.fda.gov |
| Guangzhou Ekai Electronic Technology Co.,ltd. | guangzhou Guangdong, China | Contract manufacturer, Manufacturer | 1 | August 11, 2023 | 0 | 0 | 0 | api.fda.gov |
| Beijing Beautemax Technology Limited | Beijing, China | Foreign private label distributor, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beijing Perfectlaser Technology Co.,ltd | Beijing, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beijing Winkonlaser Technology Limited | Beijing, China | Foreign private label distributor, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hebei Lufen Tech Co., Limited | Xingtai Hebei, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pan-International Precision Electronic Co., Ltd. | Dongguan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sanhe Jumei Technology Co.,ltd | Sanhe Hebei, 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.