Data / Medical devices / Media, Coupling, Ultrasound / China
FDA-registered makers of Media, Coupling, Ultrasound in China: 5 establishments
5 establishments in China are registered with the FDA to make Media, Coupling, Ultrasound (product code MUI). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Media, Coupling, Ultrasound
- Product code
- MUI
- Country
- China
Makers of Media, Coupling, Ultrasound in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Anhui Deepblue Medical Technology Co., Ltd. | Hefei Anhui, China | Manufacturer | 1 | September 19, 2024 | 0 | 0 | 0 | api.fda.gov |
| Foshan Pingchuang Medical Technology Co., Ltd | Foshan City Guangdong, China | Manufacturer | 1 | June 17, 2026 | 0 | 0 | 0 | api.fda.gov |
| Hony Medical Co., Ltd | Taishan Guangdong, China | Contract manufacturer, Manufacturer | 1 | July 24, 2024 | 0 | 0 | 0 | api.fda.gov |
| Jianerkang Medical Co., Ltd. | Changzhou City Jiangsu, China | Manufacturer | 1 | December 15, 2023 | 0 | 0 | 0 | api.fda.gov |
| Ming Fai Industrial (shenzhen) Co. Ltd. | SHENZHEN Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.