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Data / Medical devices / China / Zhongshan Kingdom Electrical Appliance Co., Ltd.

Zhongshan Kingdom Electrical Appliance Co., Ltd.: FDA-registered device maker in Zhongshan Guangdong, China, 1 510(k) clearance

Zhongshan Kingdom Electrical Appliance Co., Ltd. is registered with the FDA (registration 3013689783) in Zhongshan Guangdong, China. It lists 11 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 26, 2018. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch Zhongshan Kingdom Electrical Appliance Co., Ltd.
FDA registration number
3013689783
Address
No. 32 Jinhong Road, Pingnan Industrial Park, Sanxiang Town, Zhongshan Guangdong, China, 528463
Owner or operator
Zhongshan Kingdom Electrical Appliance Co., Ltd. (10058779)
Roles
Exporter to the US, Manufacturer
First device listed
October 27, 2018
Registered through
2026
Brand names listed
(KD2335, KD2328, KD233, KD2337, KD2331, EB-2328A, DL015, DL008), (KD520A, KD169A, KD2331-1, KD2333S, K33c, K33s, KD237, K2338SA, K2338A, K238A, K238, KD23317, KD23316, KD232, KD23313), (KD813A, KD813B, KD208, KD208A, KD815A, KD819, KD202, KD886A, KD886B, KD883A, KD883B, KD811, KD811A, KD880A, KD880B), (KD881A, D882A, ML007, DL004), Blackhead remover; Dove Ultrasonic Scrubber (KD8025X, KD8023, KD8023A, KD8026, KD803, ML006), Blackhead remover; Dove Ultrasonic Scrubber (KD803P, KD802P, KD802, KD803A, KD803S, KD8010, KD8020, KD8070, KD8022A), Facial Brush; Silicone Facial Brush (KD308X, KD308B, KD3033S, KD3033C, KD303), Facial cleanser (KD307S) and more

Devices it lists

DeviceProduct codeClassRoleSource
Adaptor, GroomingILW1Exporter to the US, Manufactureraccessdata.fda.gov
Adhesive Backed Thermal Skin PatchesOMW1Exporter to the US, Manufactureraccessdata.fda.gov
Brush, Dermabrasion, PoweredGFE1Exporter to the US, Manufactureraccessdata.fda.gov
Cabinet, Moist SteamIMB2Exporter to the US, Manufactureraccessdata.fda.gov
Epilator, High Frequency, Tweezer-TypeKCX1Exporter to the US, Manufactureraccessdata.fda.gov
Humidifier, Non-Direct Patient Interface (Home-Use)KFZ1Exporter to the US, Manufactureraccessdata.fda.gov
Light Based Over The Counter Wrinkle ReductionOHS2Exporter to the US, Manufactureraccessdata.fda.gov
Massager, Therapeutic, ElectricISA1Exporter to the US, Manufactureraccessdata.fda.gov
Over-The-Counter Powered Light Based Laser For AcneOLP2Exporter to the US, Manufactureraccessdata.fda.gov
Stimulator, Transcutaneous Electrical, Aesthetic PurposesNFO2Exporter to the US, Manufactureraccessdata.fda.gov
Unit, Heating, PoweredIRQ1Exporter 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
April 26, 2018K1718212 Face / Face EvolutionNFOSubstantially EquivalentHeat IN A Clickaccessdata.fda.gov

Compare with other makers

Updated April 26, 2018. 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.