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Data / Medical devices / China / Shenzhen Deliduo Medical Technology Co., Ltd

Shenzhen Deliduo Medical Technology Co., Ltd: FDA-registered device maker in Shenzhen City Guangdong, China, 1 510(k) clearance

Shenzhen Deliduo Medical Technology Co., Ltd is registered with the FDA (registration 3019865183) in Shenzhen City Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 15, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3019865183
Address
Room B1406, Block B, Phase 3, Hongji Garden, Center City Area 4, Jixiang Community Longcheng Street, Longgang District, Shenzhen City Guangdong, China, 518116
Owner or operator
ShenZhen Deliduo Medical Technology Co., Ltd (10092564)
Roles
Exporter to the US, Manufacturer
First device listed
January 21, 2025
Registered through
2026
Brand names listed
Cutaneous Electrode

Devices it lists

DeviceProduct codeClassRoleSource
Electrode, CutaneousGXY2Exporter to the US, 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
January 15, 2025K241512Electrode PadGXYSubstantially EquivalentShenzhen Deliduo Medical Technology Co.,Ltdaccessdata.fda.gov

Compare with other makers

Updated January 15, 2025. 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.