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Data / Medical devices / China / ECO Medical Technology (Nanjing) Co., Ltd.

ECO Medical Technology (Nanjing) Co., Ltd.: FDA-registered device maker in Nanjing Jiangsu, China, 2 510(k) clearances

ECO Medical Technology (Nanjing) Co., Ltd. is registered with the FDA (registration 3020309549) in Nanjing Jiangsu, China. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated July 23, 2021. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3020309549
Address
No.19, Xinghui Road, Jiangbei New District, Nanjing Jiangsu, China, 211500
Owner or operator
ECO Medical Technology (Nanjing) Co., Ltd. (10082450)
Roles
Exporter to the US, Manufacturer
First device listed
July 29, 2021
Registered through
2026
Brand names listed
Disposable Microwave Therapeutic Antennas ECO-100AI1, ECO-100CL28C, ECO-100CL27C, ECO-100CL22C, ECO-100CL5, ECO-100AI3, ECO-100AI18C, ECO-100AI25, ECO-100AI30, ECO-100CL29, ECO-100AL29, ECO-100CL31, ECO-100CL5C, ECO-100AL23C, ECO-100AL13C, ECO-100CL11C, ECO-100CL10, ECO-100CL10C, ECO-100CL8, ECO-100CL8C, ECO-100AI26, Microwave Therapeutic System SABERWAVE ECO-200G

Devices it lists

DeviceProduct codeClassRoleSource
System, Ablation, Microwave And AccessoriesNEY2Exporter 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
July 23, 2021K201265Disposable Microwave Therapeutic AntennasNEYSubstantially EquivalentNanjing Eco Microwave System Co., Ltd.accessdata.fda.gov
July 9, 2021K201262Microwave Therapeutic SystemNEYSubstantially EquivalentNanjing Eco Microwave System Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated July 23, 2021. 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.