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Data / Medical devices / China / Shenzhen Bestpad Technology Development Co., Ltd

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

Shenzhen Bestpad Technology Development Co., Ltd is registered with the FDA (registration 3015531976) in Shenzhen Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 14, 2019. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3015531976
Address
Block 1, Building 3, 11 Lougang Avenue Lougang Community, Songgang Street, Bao an, Shenzhen Guangdong, China, 518105
Owner or operator
Shenzhen Bestpad Technology Development Co., Ltd (10060739)
Roles
Manufacturer
First device listed
June 21, 2019
Registered through
2026
Brand names listed
ELECTRODES PAD

Devices it lists

DeviceProduct codeClassRoleSource
Electrode, CutaneousGXY2Manufactureraccessdata.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
June 14, 2019K190700ELECTRODES PADGXYSubstantially EquivalentShenzhen Bestpad Technology Development Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated June 14, 2019. 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.