Data / Medical devices / Tube, Tracheal (W/Wo Connector) / China
FDA-registered makers of Tube, Tracheal (W/Wo Connector) in China: 8 establishments
8 establishments in China are registered with the FDA to make Tube, Tracheal (W/Wo Connector) (product code BTR). 6 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Tube, Tracheal (W/Wo Connector)
- Product code
- BTR
- Country
- China
Makers of Tube, Tracheal (W/Wo Connector) in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Well Lead Medical Co. Ltd | GUANGZHOU Guangdong, China | Contract manufacturer, Manufacturer | 5 | July 21, 2022 | 0 | 1 | 0 | api.fda.gov |
| Chilecom Medical Devices Co Ltd | Xiangtan Hunan, China | Manufacturer | 1 | February 13, 2009 | 0 | 0 | 0 | api.fda.gov |
| Jiangsu Weikang Jiejing Medical Apparatus Co., Ltd. | Shuyang Jiangsu, China | Manufacturer | 1 | December 18, 2014 | 0 | 0 | 0 | api.fda.gov |
| Jiangxi Yikang Medical Instrument Group Co., Ltd. | Nanchang Jiangxi, China | Contract manufacturer, Manufacturer | 1 | September 6, 2019 | 0 | 0 | 0 | api.fda.gov |
| Tianjin Medis Medical Device Co., Ltd. | Tianjin, Tianjin, China | Manufacturer, Specification developer | 1 | April 7, 2017 | 0 | 0 | 0 | api.fda.gov |
| Well Lead Medical Co. Ltd | GUANGZHOU Guangdong, China | Manufacturer | 1 | July 10, 2008 | 0 | 0 | 0 | api.fda.gov |
| Flexicare Medical (dongguan) Ltd. | DONGGUAN CITY Guangdong, 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 |
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.