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Data / Medical devices / China / Fuzhou Xiaoyi Electronics Co., Ltd.

Fuzhou Xiaoyi Electronics Co., Ltd.: FDA-registered device maker in Fuzhou Fujian, China, 1 510(k) clearance

Fuzhou Xiaoyi Electronics Co., Ltd. is registered with the FDA (registration 3045030482) in Fuzhou Fujian, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 7, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3045030482
Address
Room 1302, No. 118 Shuguang Road, Taijiang District, Fuzhou, Fujian, China, Fuzhou Fujian, China, 350018
Owner or operator
Fuzhou Xiaoyi Electronics Co., Ltd. (10095653)
Roles
Exporter to the US
First device listed
April 8, 2026
Registered through
2026
Brand names listed
BladGo 2, BladGo 2 bladder scanner

Devices it lists

DeviceProduct codeClassRoleSource
System, Imaging, Pulsed Echo, UltrasonicIYO2Exporter to the USaccessdata.fda.gov
Transducer, Ultrasonic, DiagnosticITX2Exporter to the USaccessdata.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
July 7, 2023K223448Bladder Scanner Model: BVT02IYOSubstantially EquivalentXuzhou Kaixin Electronic Instrument Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated July 7, 2023. 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.