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

Shenzhen Yingchi Technology Co., Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 4 510(k) clearances

Shenzhen Yingchi Technology Co., Ltd. is registered with the FDA (registration 3029767018) in Shenzhen Guangdong, China. It lists 3 device types. The FDA files 4 510(k) clearances under its listings, the newest dated August 14, 2026. 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
3029767018
Address
Block A, 2/F, Phoenix City Building, 15 Sci Tech North 1st Road, Xili, Shenzhen Guangdong, China, 518057
Owner or operator
Shenzhen Yingchi Technology Co., Ltd. (10088708)
Roles
Manufacturer
First device listed
October 4, 2023
Registered through
2026
Brand names listed
QuickVision Ultimate rTMS, QuickVision Yingchi rTMS, Ultimate rTMS, Ultimate rTMS for MDD (iTBS), Ultimate rTMS for OCD, Yingchi rTMS, Yingchi rTMS for MDD (iTBS), Yingchi rTMS for OCD

Devices it lists

DeviceProduct codeClassRoleSource
Extracranial Positional System For A Transcranial Magnetic Stimulation SystemSGE2Manufactureraccessdata.fda.gov
Transcranial Magnetic Stimulation System For Obsessive-Compulsive DisorderQCI2Manufactureraccessdata.fda.gov
Transcranial Magnetic StimulatorOBP2Manufactureraccessdata.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
August 14, 2026K261228QuickVision Ultimate rTMSOBPSubstantially EquivalentBrain Ultimate, Inc.accessdata.fda.gov
April 17, 2025K243460Ultimate rTMSOBPSubstantially EquivalentBrain Ultimate, Inc.accessdata.fda.gov
April 17, 2025K243459Ultimate rTMS for OCD (M-series)QCISubstantially EquivalentBrain Ultimate, Inc.accessdata.fda.gov
September 13, 2023K230735Ultimate rTMS; Yingchi rTMSOBPSubstantially EquivalentBrain Ultimate, Inc.accessdata.fda.gov

Compare with other makers

Updated August 14, 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.