Data / Medical devices / Gas, Laser Generating / China
FDA-registered makers of Gas, Laser Generating in China: 16 establishments
16 establishments in China are registered with the FDA to make Gas, Laser Generating (product code NXF). 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
- Gas, Laser Generating
- Product code
- NXF
- Country
- China
Makers of Gas, Laser Generating in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Beijing Beautemax Technology Limited | Beijing, China | Foreign private label distributor, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beijing Goldenlaser Development Co., Ltd. | Beijing, China | 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 | |
| Beijing Nubway S&T Co.,Ltd. | Beijing, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Changsha Gomecy Electronics Co., Ltd. | Changsha Hunan, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Foshan Xinnuo Medical Equipment Co., Ltd | Foshan Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Foshan Zike Technology Co., Ltd. | Foshan Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangdong Fuqiang Beauty Equipment Co.,limited | Qingyuan Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hebei Lufen Tech Co., Limited | Xingtai Hebei, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hebei Tuosite Technology Co.,ltd | Shijiazhuang Hebei, China | 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 | |
| Sanhe Meditech Co., Ltd | Sanhe Hebei, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Svenson Network Holdings Limited | HK Hong Kong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shandong Moonlight Electronics Tech Co.,Ltd. | Weifang Shandong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Weifang Dragonfly Electronic Technology Co., Ltd. | Weifang Shandong, China | 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.