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Data / Medical devices / China / Shenzhen Xiazhifeng Electronic Co., Ltd

Shenzhen Xiazhifeng Electronic Co., Ltd: FDA-registered device maker in Shenzhen Guangdong, China, 2 510(k) clearances

Shenzhen Xiazhifeng Electronic Co., Ltd is registered with the FDA (registration 3015989868) in Shenzhen Guangdong, China. It lists 25 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 20, 2026. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3015989868
Address
4th Floor, Building A2, No. 2, Yanhe Road, Xinsheng Community, Longgang Sub-district, Longgang District, Shenzhen Guangdong, China, 518116
Owner or operator
Shenzhen Xiazhifeng Electronic Co., Ltd (10061503)
Roles
Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler
First device listed
October 23, 2019
Registered through
2027
Brand names listed
Anti Snore Device, Body Massager Device,shoulder Massager,neck Massager, leg Massager,hand Massager, Body correction belt, Body massage gun, Chest massager, DPL Skin Rejuvenation Beauty Instrument, Dental floss: WG-FY-B801, EMS Beauty Device and more

Devices it lists

DeviceProduct codeClassRoleSource
Adaptor, GroomingILW1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Adaptor, HygieneILS1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Analyzer, Body Composition, ExemptPUH2Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Brush, Dermabrasion, PoweredGFE1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Cleaner, Denture, MechanicalJER1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Clip, NoseBXJ1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Curette, EarJYG1Exporter to the US, Manufacturer, Repackager or relabeleraccessdata.fda.gov
Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical UseLXG1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Floss, DentalJES1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Gauze / Sponge,Nonresorbable For External UseNAB1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Humidifier, Non-Direct Patient Interface (Home-Use)KFZ1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Intraoral CameraQJK2Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Irrigator, Powered NasalKMA1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Lamp, Infrared, Therapeutic HeatingILY2Manufactureraccessdata.fda.gov
Light Based Over-The-Counter Hair RemovalOHT2Manufactureraccessdata.fda.gov
Massager, Therapeutic, ElectricISA1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Needle, Tumor LocalizationMIJ1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Orthosis, Limb BraceIQI1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Orthosis, LumbarIQE1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Pick, MassagingJET1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
RaspHTR1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Thermometer KitPXH2Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Toothbrush, PoweredJEQ1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Tray, Impression, PreformedEHY1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Unit, Oral IrrigationEFS1Contract manufacturer, Exporter 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
May 20, 2026K260594IPL Hair Removal Device (FL-B505AG, FL-B505AP, FL-B505AM, FL-B507AG, FL-B507AP, FL-B507AM, FL-B508AG, FL-B508AP, FL-B508AM, FL-B509AG, FL-B509AP, FL-B509AM, FL-B510G, FL-B510P, FL-B510M, FL-B511G, FL-B511P, FL-B511M, FL-B512AG, FL-B512AP, FL-B512AM, FL-B513AG, FL-B513AP, FL-B513AM)OHTSubstantially EquivalentShenzhen Xiazhifeng Electronic Co., Ltd.accessdata.fda.gov
April 25, 2023K230549IPL Hair Removal Device, Model(s): FY-B505AL, FY-B505AG, FY-B505BL, FY-B505BG, FY-B507AL, FY-B507AG, FY-B507BL, FY-B507BG, FY-B508AL, FY-B508AG, FY-B508BL, FY-B508BG, FY-B509AL, FY-B509AG, FY-B509BL, FY-B509BGOHTSubstantially EquivalentShenzhen Xiazhifeng Electronic Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated May 20, 2026. 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.