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

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

Shenzhen Enmind Technology Co., Ltd. is registered with the FDA (registration 3043745121) in Shenzhen Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 2, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3043745121
Address
Room 201, Block A, No.1, Qianhai Road 1, Qianhaishen Port Cooperative District, Shenzhen Guangdong, China, 518000
Owner or operator
Shenzhen Enmind Technology Co., Ltd. (10095217)
Roles
Manufacturer
First device listed
February 6, 2026
Registered through
2026
Brand names listed
IPL Hair Removal Device (IPL-001, IPL-002)

Devices it lists

DeviceProduct codeClassRoleSource
Light Based Over-The-Counter Hair RemovalOHT2Manufactureraccessdata.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
October 2, 2025K251398IPL Hair Removal Device (IPL-001, IPL-002)OHTSubstantially EquivalentShenzhen Enmind Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated October 2, 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.