Data / Medical devices / Valve, Non-Rebreathing / China
FDA-registered makers of Valve, Non-Rebreathing in China: 11 establishments
11 establishments in China are registered with the FDA to make Valve, Non-Rebreathing (product code CBP). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Valve, Non-Rebreathing
- Product code
- CBP
- Country
- China
Makers of Valve, Non-Rebreathing in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| FIRSTAR HEALTHCARE Company Limited (Guangzhou) | Guangzhou Guangdong, China | Exporter to the US, Manufacturer | 2 | November 25, 2020 | 0 | 0 | 0 | api.fda.gov |
| Laerdal Medical (suzhou) Co., Ltd. | 215009 Suzhou Jiangsu Province, China | Manufacturer | 2 | February 11, 2003 | 0 | 0 | 0 | api.fda.gov |
| Medsource Factory,inc. | CHANGZHOU Jiangsu, China | Manufacturer | 2 | August 26, 2008 | 0 | 0 | 0 | api.fda.gov |
| Dongguan City Ruimi Gift Products Co Ltd | Dongguan Guangdong, China | Exporter to the US, Manufacturer | 1 | November 17, 2017 | 0 | 0 | 0 | api.fda.gov |
| Xiamen Compower Medical Tech. Co., Ltd. | Xiamen Fujian, China | Manufacturer | 1 | November 17, 2017 | 0 | 0 | 0 | api.fda.gov |
| Flying Tooling Engineering Limited | Dongguan 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 | |
| Hangzhou Jinlin Medical Appliances Co., Ltd. | Hangzhou Zhejiang, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Polymed (xiamen) Plastic Industrial Co.,ltd. | XIAMEN Fujian, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Saferlife Products Co.,ltd. | Guangzhou Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Xiamen Tianzuo Medical Co., Ltd. | Xiamen Fujian, 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.