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Data / Medical devices / China / Shenzhen Ulike Smart Electronics Co.,ltd

Shenzhen Ulike Smart Electronics Co.,ltd: FDA-registered device maker in Shenzhen Guangdong, China, 17 510(k) clearances

Shenzhen Ulike Smart Electronics Co.,ltd is registered with the FDA (registration 3023339103) in Shenzhen Guangdong, China. It lists 6 device types. The FDA files 17 510(k) clearances under its listings, the newest dated May 21, 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
3023339103
Address
810, Building 1, Xunmei Science and Technology Plaza, No. 8 Keyuan Road,, Science Park Community, Yuehai Sub-District, Nanshan District, Shenzhen Guangdong, China, 518000
Owner or operator
Shenzhen Ulike Smart Electronics Co.,Ltd (10085336)
Roles
Manufacturer, Specification developer
First device listed
June 5, 2022
Registered through
2026
Brand names listed
Diamond Air+, IPL Hair Removal Device, Model(S):, IPL Hair Removal Device, Model(S):, IPL Hair Removal Device, Model(S):UI06 PN, UI06 BR, UI06 PR, UI06 WH, UI06 PL, UI06 JL, UI06 DB, UI06 OG,, IPL Safety Glasses, Goggles, Safety Goggles, Ice Cooling IPL Hair Removal Device, Ice Cooling IPL Hair Removal Device, Model(S): UIM20 GR, UIM20 BK, UIM20 SL, UIM20 CB, UIM20 WR, Ice Cooling IPL Hair Removal Device;, Ice Cooling IPL Hair Removal Device; Model(S): UI20 DB, UI20 RE, UI20 GP, UI20 PW, UI20S DB, UI20S RE, UI20S PW, 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 21, 2026K261325Ice Cooling IPL Hair Removal Device (UI06S PR, UI06S PN, UI06S WH, UI06S PRU, UI06S PNU, UI06S WHU)OHTSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov
May 5, 2026K260742Ice Cooling IPL Hair Removal Device (UI20S DB, UI20S RE, UI20S PW, UI20S GP, UI20S GR, UI20S BK)OHTSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov
March 16, 2026K260511Ulike Reglow Light Therapy Device (UM10)OHSSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov
October 1, 2025K252804Ice Cooling IPL Hair Removal Device (UI20S BK, UI20S BS, UI20S DB, UI20S GP, UI20S GR, UI20S MP, UI20S PW, UI20S RE, UI20S WH, UI20WG;UI20 BK, UI20 BL, UI20 BR, UI20 BS, UI20 DB, UI20 GP, UI20 GR, UI20 MP, UI20 PN, UI20 PW, UI20 RE, UI20 WH; UI06 PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB,UI06 PR, UI06 OG,UI06RD,UI06 WH, UI06 MG, UI06 OB, UI06 LY, UI06 IG; UI06S PR, UI06S PN, UI06S WH, UI06S PRU, UI06S PNU, UI06S WHU; UI04 MK, UI04 BN, UI04 BU, UI04 CB, UI04 GY, UI04 LG, UI04 DG, UI04 PL,OHTSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov
October 1, 2025K251825Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)OHSSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov
May 23, 2025K250938Ice Cooling IPL Hair Removal Device (MI01 LP, MI01 CB, MI01 GR, MI01 PP, MI01 RM, MI01 WG, MI01 WH, MI01 BK;UI04S PP, UI04S BU, UI04S WH, UI04S PN)OHTSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov
April 8, 2025K243749Jmoon Conductive GelGYBSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov
March 26, 2025K250194Ice Cooling IPL Hair Removal Device (UI06S PR, UI06S PN, UI06S WH)OHTSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov
February 3, 2025K243393JMOON NouvelleSkin Facial Toning Device (M30U PR, M30U MW, M30U SG, M30U SK, M30U MP)NFOSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov
January 10, 2025K243492Ulike Reglow Light Therapy Device (UM10)OHSSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov
December 13, 2024K241998Ice Cooling IPL Hair Removal Device (UI20 DB, UI20 RE, UI20 GP, UI20 PW, UI20S DB, UI20S RE, UI20S PW, UI20S GP,UI20 WH, UI20 GR, UI20 BS, UI20 MP, UI20 BL, UI20 PN, UI20 BR, UI20WG, UI20S WH, UI20S GR, UI20S BS, UI20S MP)OHTSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov
November 6, 2024K242039Ice Cooling IPL Hair Removal Device (UIM20 GR, UIM20 BK, UIM20 SL, UIM20 CB, UIM20 WR)OHTSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov
April 4, 2024K240652Ice Cooling IPL Hair Removal Device (UI06 PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB, UI06 PR, UI06 OG,UI06 RD,UI06 WH, UI06 MG, UI06 OB, UI06 LY, UI06 IG, UIM20 GR, UIM20 BK, UIM20 SL, UIM20 CB, UIM20 WR)OHTSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov
January 11, 2024K233664IPL Hair Removal Device (UI06 PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB, UI06 PR, UI06 OG, UI06 RD,UI06 WH, UI06 MG, UI06 OB, UI06 LY,UI06 IG,)OHTSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov
January 5, 2024K233679IPL Hair Removal Device (UI04 MK,UI04 BN,UI04 BU,UI04 CB,UI04 GY,UI04 LG,UI04 DG,UI04 PL,UI04 PN,UI04 SD,UI04 SG,UI04 MG)OHTSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov
April 10, 2023K230122IPL Hair Removal Device, Model(s): UI04 SD, UI04 DGOHTSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov
June 1, 2022K221002IPL Hair Removal Device, Model(s): UI04A, UI04B, UI04COHTSubstantially EquivalentShenzhen Ulike Smart Electronics Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated May 21, 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.