Data / Medical devices / Light, Surgical, Ceiling Mounted / China
FDA-registered makers of Light, Surgical, Ceiling Mounted in China: 5 establishments
5 establishments in China are registered with the FDA to make Light, Surgical, Ceiling Mounted (product code FSY). 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
- Light, Surgical, Ceiling Mounted
- Product code
- FSY
- Country
- China
Makers of Light, Surgical, Ceiling Mounted in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Beijing Aeonmed Co., Ltd. | Sanhe Hebei, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangdong Kareway Medical Technology Co., Ltd | Foshan Guangdong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nanchang Micare Medical Equipment Co.,ltd | Nanchang Jiangxi, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shandong Deman Medical Equipment Group Co., Ltd | Jining City Shandong, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Kaiyan Medical Equipment Co., Ltd | Shenzhen Guangdong, China | Contract 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.