Data / Medical devices / Humidifier, Respiratory Gas, (Direct Patient Interface) / China
FDA-registered makers of Humidifier, Respiratory Gas, (Direct Patient Interface) in China: 11 establishments
11 establishments in China are registered with the FDA to make Humidifier, Respiratory Gas, (Direct Patient Interface) (product code BTT). 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
- Humidifier, Respiratory Gas, (Direct Patient Interface)
- Product code
- BTT
- Country
- China
Makers of Humidifier, Respiratory Gas, (Direct Patient Interface) in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Chinamed Products (china) Ltd. | Gaoyao District Guangdong, China | Manufacturer | 1 | August 25, 2016 | 0 | 0 | 0 | api.fda.gov |
| Vincent Medical(dongguan)technology Company Limited | Dongguan Guangdong, China | Manufacturer | 1 | December 21, 2022 | 0 | 0 | 0 | api.fda.gov |
| Beijing Aeonmed Co., Ltd. | Sanhe Hebei, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Betacera Inc. | Suzhou City Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Flexicare Medical (dongguan) Ltd. | DONGGUAN CITY Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GaleMed (Xiamen) Co., Ltd. | XIAMEN Fujian, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jianerkang Medical Co., Ltd. | Changzhou City Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ninghai Guangjie Electronic Commerce Co., Ltd | Ningbo Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shenzhen Med-Link Electronics Tech Co.,ltd | Shenzhen Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sunmed Ap, Ltd. | ZHUHAI Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vincent Medical (dong Guan) Manufacturing Co., Ltd. | Dong Guan City 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.