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Data / Medical devices / China / Guangdong Youmeng Electrical Technology Co., Ltd.

Guangdong Youmeng Electrical Technology Co., Ltd.: FDA-registered device maker in Foshan Guangdong, China, 4 510(k) clearances

Guangdong Youmeng Electrical Technology Co., Ltd. is registered with the FDA (registration 3030479957) in Foshan Guangdong, China. It lists 3 device types. The FDA files 4 510(k) clearances under its listings, the newest dated August 20, 2026. Registered through 2027. 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
3030479957
Address
One of Area A, level 3, Building 2, No. 17,Keyuan 3rd Road,Xiaohuangpu Community, Ronggui Street,Shunde District,Foshan City, Guangdong Province, China, Foshan Guangdong, China, 528303
Owner or operator
Guangdong Youmeng Electrical Technology Co., Ltd. (10089995)
Roles
Contract manufacturer, Manufacturer
First device listed
January 31, 2024
Registered through
2027
Brand names listed
Electrc Breast Pump, Electric Breast Pump, Manual Breast Pump, PC Manual Breast Pump, Philips Avent Natural Care Hands-free Wearable Electric Breast Pump (Model: SCF593/52, SCF593/62);, Philips Avent Natural Care Warming Hands-free Wearable Electric Breast Pump (Model: SCF594/52, SCF594/62), Wearable Electric Breast Pump, Wearable Electric Breast Pump(Melody InBra™ YM-8803) and more

Devices it lists

DeviceProduct codeClassRoleSource
Breast Pump KitOHH2Manufactureraccessdata.fda.gov
Pump, Breast, Non-PoweredHGY1Manufactureraccessdata.fda.gov
Pump, Breast, PoweredHGX2Contract manufacturer, Manufactureraccessdata.fda.gov

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
August 20, 2026K261298Wearable Electric Breast Pump (YM-8837, YM-8838, YM-8856(H03), YM-8809(S42))HGXSubstantially EquivalentGuangdong Youmeng Electrical Technology Co., Ltd.accessdata.fda.gov
December 19, 2025K252754Wearable Electric Breast Pump (YM-8803)HGXSubstantially EquivalentGuangdong Youmeng Electrical Technology Co., Ltd.accessdata.fda.gov
December 19, 2025K252342Electric Breast Pump (YM-8807, YM-8805, YM-8806, YM-8810)HGXSubstantially EquivalentGuangdong Youmeng Electrical Technology Co., Ltd.accessdata.fda.gov
January 19, 2024K232466Electric Breast Pump, model: YM-8166HGXSubstantially EquivalentGuangdong Youmeng Electrical Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated August 20, 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.