Data / Medical devices / Flowmeter, Tube, Thorpe, Back-Pressure Compensated / China
FDA-registered makers of Flowmeter, Tube, Thorpe, Back-Pressure Compensated in China: 9 establishments
9 establishments in China are registered with the FDA to make Flowmeter, Tube, Thorpe, Back-Pressure Compensated (product code CAX). 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
- Flowmeter, Tube, Thorpe, Back-Pressure Compensated
- Product code
- CAX
- Country
- China
Makers of Flowmeter, Tube, Thorpe, Back-Pressure Compensated in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Danyang Xinya Valve Co., Ltd. | Danyang Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Foshan Kycare Medical Equipment Co. Ltd | Foshan City Guangdong, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gentec (shanghai) Corporation | Shanghai, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Longfian Scitech Co., Ltd. | Baoding Hebei, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nantong Kangjinchen Medical Equipment Co., Ltd. | Nantong Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ningbo Jiangbei Tenso Medical Instruments Co., Ltd | NINGBO Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Suzhou Meccan Import and Export Corp. | Suzhou Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Univac Precision Plastics (suzhou) Co.,ltd | Suzhou Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zhejiang Mediunion Healthcare Group Co.,ltd | Ningbo Zhejiang, 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.