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Data / Medical devices / China / Shenzhen Xinrun Electric Appliances Co Ltd

Shenzhen Xinrun Electric Appliances Co Ltd: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance

Shenzhen Xinrun Electric Appliances Co Ltd is registered with the FDA (registration 3010246951) in Shenzhen Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 22, 2013. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3010246951
Address
Shenzhen Boan District, Shajing Street, Wanan Rd, Changxing Technology Park, No13, RM 401, RM 501, Shenzhen Guangdong, China, 518104
Owner or operator
Shenzhen Xinrun Electric Appliances Co Ltd (10043608)
Roles
Contract manufacturer, Manufacturer
First device listed
March 4, 2013
Registered through
2026
Brand names listed
VPULSE SYSTEM

Devices it lists

DeviceProduct codeClassRoleSource
Sleeve, Limb, CompressibleJOW2Contract manufacturer, 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
February 22, 2013K122640VPULSEJOWSubstantially EquivalentCothera, LLCaccessdata.fda.gov

Compare with other makers

Updated February 22, 2013. 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.