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Data / Medical devices / China / Jiangxi Aov Maternity & Baby Products Co., Ltd.

Jiangxi Aov Maternity & Baby Products Co., Ltd.: FDA-registered device maker in Yingtan City Jiangxi, China, 2 510(k) clearances

Jiangxi Aov Maternity & Baby Products Co., Ltd. is registered with the FDA (registration 3016871906) in Yingtan City Jiangxi, China. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated April 22, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3016871906
Address
No. 8, Nanhuan Road, Industrial Park, Guixi, Yingtan City Jiangxi, China, 335000
Owner or operator
Jiangxi AOV Maternity & Baby Products Co., Ltd. (10093742)
Roles
Manufacturer
First device listed
July 1, 2025
Registered through
2026
Brand names listed
AOV Wearable Breast Pump AOV6853, AOV Wearable Breast Pump AOV6860, AOV Wearable Breast Pump AOV6861, AOV Wearable Breast Pump AOV6862, Electric Breast Pump (Models AOV6818, AOV6821, AOV6826, AOV6830, AOV6852), K8

Devices it lists

DeviceProduct codeClassRoleSource
Pump, Breast, PoweredHGX2Manufactureraccessdata.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
April 22, 2026K260239Wearable Breast Pump (AOV6853, AOV6860, AOV6861, AOV6862)HGXSubstantially EquivalentJiangxi AOV Maternity & Baby Products Co., Ltd.accessdata.fda.gov
May 9, 2024K232477Electric Breast Pump (Models AOV6818, AOV6821, AOV6826, AOV6830, AOV6852)HGXSubstantially EquivalentJiangxi AOV Maternity & Baby Products Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated April 22, 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.