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Data / Medical devices / China / Dongguan Lide Electric Appliance Co., Ltd

Dongguan Lide Electric Appliance Co., Ltd: FDA-registered device maker in Dongguan Guangdong, China, 2 510(k) clearances

Dongguan Lide Electric Appliance Co., Ltd is registered with the FDA (registration 3029992391) in Dongguan Guangdong, China. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 25, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3029992391
Address
Floor 4, Building 2, No.11 Yinhe Fifth Road, Qiaotou Town, Dongguan Guangdong, China, 523528
Owner or operator
Dongguan Lide Electric Appliance Co., Ltd (10088875)
Roles
Manufacturer
First device listed
October 18, 2023
Registered through
2026
Brand names listed
Graphene FIR Helmet LD-SF01,LD-SF02,LD-SF03,LD-SF04,LD-SF05,LD-SF06,LD-SF07,LD-SF08,LD-SF09,LD-SF10, IPL Hair Removal Device (Models: KA-10, KA-11, KA-11C, KA-11D, KA-18, KA-20, KA-21, KA-21C), IPL Hair Removal Device (Models: PB1, PB2, PB3, PB4, TM002), LED Red Therapy Light LD-DPD01,LD-DPD02,LD- DPD03,LD-DPD04,LD-DPD05,LD-DPD06,LD- DPD07,LD-DPD08,LD-DPD09,LD-DPF10

Devices it lists

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
November 25, 2025K253304IPL Hair Removal Device (KA-10, KA-11, KA-11C, KA-11D, KA-18, KA-20, KA-21, KA-21C)OHTSubstantially EquivalentDongguan Lide Electric Appliance Co., Ltd.accessdata.fda.gov
October 6, 2023K232056IPL Hair Removal Device, Model(s): PB1, PB2, PB3, PB4, TM002OHTSubstantially EquivalentDongguan Lide Electric Appliance Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated November 25, 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.