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Data / Medical devices / China / Shenzhen Zhenxing Ruitong Technology Co., Ltd.

Shenzhen Zhenxing Ruitong Technology Co., Ltd.: FDA-registered device maker in shenzhen Guangdong, China, 1 510(k) clearance

Shenzhen Zhenxing Ruitong Technology Co., Ltd. is registered with the FDA (registration 3033850489) in shenzhen Guangdong, China. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 17, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3033850489
Address
Room 25C, Microsoft Science and Technology Building, Nanshan District, Shenzhen City, Guangdong Province, shenzhen Guangdong, China, 518000
Owner or operator
Shenzhen Zhenxing Ruitong Technology Co., Ltd. (10091736)
Roles
Specification developer
First device listed
October 29, 2024
Registered through
2026
Brand names listed
Abs Massage Belt (ME2), Arm Massage Belt (ME1), EMS Heated Neck Massage Pillow (7C-AM-10), EMS Trainer for Abdomen (LD-B2), EMS Trainer for Arm (LD-B1), EMS Wireless Muscle Stimulator (PM144), MEGELIN, MEGELIN LED LIGHT THERAPY MACHINE (JM094,JM095,JM096,JM097,JM098,JM099,XYO-2308,XYO-2309,XYO-2310,XYO-2311,XYO-2312) and more

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
October 17, 2025K252264MEGELIN LED Light Therapy Mask (JML1, JML1+JML2); MEGELIN LED Light Therapy Mask (JML3, JML3+JML4); MEGELIN LED Light Therapy Mask (JML5, JML5+JML7); MEGELIN LED Light Therapy Mask (JML6, JML6+JML8); MEGELIN LED Light Therapy Mask (JML9, JML9+JML10)OHSSubstantially EquivalentShenzhen Zhenxing Ruitong Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated October 17, 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.