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Data / Medical devices / China / Shenzhen Willcareyou Technology Co., Ltd

Shenzhen Willcareyou Technology Co., Ltd: FDA-registered device maker in Shenzhen Guangdong, China, 3 510(k) clearances

Shenzhen Willcareyou Technology Co., Ltd is registered with the FDA (registration 3033847811) in Shenzhen Guangdong, China. It lists 10 device types. The FDA files 3 510(k) clearances under its listings, the newest dated May 10, 2023. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3033847811
Address
Factory Building Room 501, No. 17 Furong Road, Tantou Community, Songgang Street, Bao an District, Shenzhen Guangdong, China, 518000
Owner or operator
Shenzhen Willcareyou Technology Co., Ltd (10091678)
Roles
Manufacturer, Remanufacturer
First device listed
October 23, 2024
Registered through
2026
Brand names listed
LED Facial Mask with Ice compress, Laser Hair Growth Cap, Led Light Therapy Foot Machine, Rehabilitation Robot Gloves RRG-100, RRG-120, RRG-HT200, RRG-210, RRG-220;, Rehabilitation Robot Gloves RRG-300, RRG-310, RRG-320, RRG-330, RRG-330N, RRG-400, Transcutaneous Electrical Nerve Stimulator(Model: KTR-4021), Transcutaneous Electrical Nerve Stimulator(Model: KTR-4026, KTR- 4034, KTR-4039,KTR-4031, KTR-4032, KTR-4032, KTR-4029), Transcutaneous Electrical Nerve Stimulator(Model: KTR-4027) 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
May 10, 2023K222870Transcutaneous Electrical Nerve Stimulator, Model: KTR-4031, KTR-4032, KTR-4012, KTR-4015, KTR-4029, KTR-4027, KTR-4026, KTR-4021, KTR-4034, KTR-4036, KTR-4037, KTR-4039NUHSubstantially EquivalentShenzhen Kentro Medical Electronics Co., Ltd.accessdata.fda.gov
May 5, 2023K230351LED Facial MaskOHSSubstantially EquivalentShenzhen Sungpo Hi-Tech Electronic Co., Ltd.accessdata.fda.gov
December 13, 2019K192627Laser Hair Growth CapOAPSubstantially EquivalentShang FA Biotechnology Co.accessdata.fda.gov

Compare with other makers

Updated May 10, 2023. 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.