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Data / Medical devices / China / Eieling Technology (shenzhen) Limited

Eieling Technology (shenzhen) Limited: FDA-registered device maker in Nanshan District, Shenzhen Guangdong, China, 3 510(k) clearances

Eieling Technology (shenzhen) Limited is registered with the FDA (registration 3033743848) in Nanshan District, Shenzhen Guangdong, China. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated February 6, 2026. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3033743848
Address
RM610, Building E, Qihang Innovation Development Park, No. 1008 Songbai Road,Yangguang Community, Xili Street, Nanshan District, Shenzhen Guangdong, China, 518055
Owner or operator
Eieling Technology (Shenzhen) Limited (10091429)
Roles
Manufacturer
First device listed
October 3, 2024
Registered through
2026
Brand names listed
Liver fat ultrasound quantitative system, Portable Liver Elastography Ultrasound Diagnostic System (Liverscan C), Portable Liver Elastography Ultrasound Diagnostic System (Liverscan Mobile), The FattaLab

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 6, 2026K253221Liver fat ultrasound quantitative system, The FattaLab (FL-CC M1, FL-CC M1_Pro)IYOSubstantially EquivalentEieling Technology (Shenzhen) Limitedaccessdata.fda.gov
November 19, 2024K242496Portable Liver Elastography Ultrasound Diagnostic System (Liverscan C)IYOSubstantially EquivalentEieling Technology (Shenzhen) Limitedaccessdata.fda.gov
February 12, 2024K233401Portable Liver Elastography Ultrasound Diagnostic System (Liverscan Mobile)IYOSubstantially EquivalentEieling Technology Limitedaccessdata.fda.gov

Compare with other makers

Updated February 6, 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.