Data / Medical devices / Monitor, Ultrasonic, Fetal / China
FDA-registered makers of Monitor, Ultrasonic, Fetal in China: 11 establishments
11 establishments in China are registered with the FDA to make Monitor, Ultrasonic, Fetal (product code KNG). 11 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
- Monitor, Ultrasonic, Fetal
- Product code
- KNG
- Country
- China
Makers of Monitor, Ultrasonic, Fetal in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Contec Medical Systems Co., Ltd | Qinhuangdao Hebei, China | Manufacturer | 3 | June 14, 2024 | 0 | 0 | 0 | api.fda.gov |
| Edan Instruments, Inc. | Shenzhen Guangdong, China | Manufacturer | 3 | June 6, 2018 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Bestman Instrument Co.,ltd | Shenzhen Guangdong, China | Exporter to the US, Manufacturer | 2 | June 26, 2025 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Jumper Medical Equipment Co.,Ltd. | Shenzhen Guangdong, China | Manufacturer | 2 | January 24, 2014 | 0 | 0 | 0 | api.fda.gov |
| Ninghai Guangjie Electronic Commerce Co., Ltd | Ningbo Zhejiang, China | Manufacturer | 1 | December 11, 1992 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Imdk Medical Technology Co., Ltd. | SHENZHEN Guangdong, China | Manufacturer | 1 | July 19, 2018 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Jamr Technology Co., Ltd | Shenzhen Guangdong, China | Manufacturer | 1 | June 28, 2024 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Taikang Medical Equipment Co.,ltd. | Shenzhen Guangdong, China | Manufacturer | 1 | January 7, 2022 | 0 | 0 | 0 | api.fda.gov |
| Shenzhen Biocare Bio-Medical Equipment Co., Ltd. | Shenzhen Guangdong, China | Manufacturer | 1 | May 21, 2010 | 0 | 0 | 0 | api.fda.gov |
| Vcomin Technology Limited | Shenzhen Guangdong, China | Manufacturer | 1 | May 29, 2019 | 0 | 0 | 0 | api.fda.gov |
| Zhongshan Xiaolan Town Senlan Electronic Factory | Zhongshan City Guangdong, China | Manufacturer | 1 | January 8, 2026 | 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.