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Data / Medical devices / China / Zhuhai Yueja Medical Device Technology Co., Ltd.

Zhuhai Yueja Medical Device Technology Co., Ltd.: FDA-registered device maker in Zhuhai Guangdong, China, 3 510(k) clearances

Zhuhai Yueja Medical Device Technology Co., Ltd. is registered with the FDA (registration 3022028624) in Zhuhai Guangdong, China. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated February 9, 2024. Registered through 2026. 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.

FDA registration number
3022028624
Address
2F, Block A, Xinaolin Science and Technology Industrial Park, High-Tech Zone, Zhuhai Guangdong, China, 519085
Owner or operator
ZHUHAI YUEJA MEDICAL DEVICE TECHNOLOGY CO., LTD. (10084598)
Roles
Manufacturer
First device listed
March 10, 2022
Registered through
2026
Brand names listed
Electronic Blood Pressure Monitor, Infrared Thermometer:Model Yj600, Luxury multifunctional massage chair, Wrist blood Pressure Monitor

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
February 9, 2024K232473Infrared Thermometer: Model YJ600FLLSubstantially EquivalentZhuhai Yueja Medical Device Technology Co., Ltd.accessdata.fda.gov
December 11, 2023K232815Wrist Blood Pressure MonitorDXNSubstantially EquivalentZhuhai Yueja Medical Device Technology Co., Ltd.accessdata.fda.gov
December 5, 2023K232814Electronic Blood Pressure MonitorDXNSubstantially EquivalentZhuhai Yueja Medical Device Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated February 9, 2024. 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.