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Data / Medical devices / China / Foshan Jindi Electric Appliance Co.,ltd

Foshan Jindi Electric Appliance Co.,ltd: FDA-registered device maker in Foshan Guangdong, China, 2 510(k) clearances

Foshan Jindi Electric Appliance Co.,ltd is registered with the FDA (registration 3029792043) in Foshan Guangdong, China. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated October 10, 2025. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3029792043
Address
No.13-2, Baiye Avenue, Xiqiao Science and Technology Industrial Park Xiqiao Town, Nanhai District, Foshan Guangdong, China, 528211
Owner or operator
Foshan Jindi Electric Appliance Co.,Ltd (10088646)
Roles
Manufacturer
First device listed
September 14, 2023
Registered through
2026
Brand names listed
IPL Hair Removal Device, IPL Home Use Hair Removal Device (Models: JD-TM016, JD-TM023, JD-TM027, JD-TM028, JD-TM032)

Devices it lists

DeviceProduct codeClassRoleSource
Light Based Over-The-Counter Hair RemovalOHT2Manufactureraccessdata.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
October 10, 2025K252209IPL Home Use Hair Removal Device (JD-TM016, JD-TM023, JD-TM027, JD-TM028, JD-TM032)OHTSubstantially EquivalentFoshan Jindi Electric Appliance Co., Ltd.accessdata.fda.gov
September 6, 2023K231717IPL Home Use Hair Removal Device, Model(s): JD-TM002, JD-TM003, JD-TM012, JD-TM016, JD-TM022OHTSubstantially EquivalentFoshan Jindi Electric Appliance Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated October 10, 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.