Data / Medical devices / Singapore / Ulike International Industrial Pte. Ltd.
Ulike International Industrial Pte. Ltd.: FDA-registered device maker in Singapore North West, Singapore, 5 510(k) clearances
Ulike International Industrial Pte. Ltd. is registered with the FDA (registration 3036720861) in Singapore North West, Singapore. It lists 5 device types. The FDA files 5 510(k) clearances under its listings, the newest dated April 8, 2025. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3036720861
- Address
- 190 Woodlands Industrial Park E5 #08-13 Woodlands Bizhub, Singapore North West, Singapore, 757516
- Owner or operator
- ULIKE INTERNATIONAL INDUSTRIAL PTE. LTD. (10092868)
- Roles
- Contract manufacturer, Exporter to the US
- First device listed
- February 28, 2025
- Registered through
- 2026
- Brand names listed
- 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,, Ice Cooling IPL Hair Removal Device, Ice Cooling IPL Hair Removal Device (UI20S DB, UI20S RE, UI20S PW, UI20S GP, UI20S GR, UI20S BK), Ice Cooling IPL Hair Removal Device, Model(S): UI06 PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB, UI06 PR, UI06 OG,UI06 RD,, Ice Cooling IPL Hair Removal Device; Model(S): UI20 DB, UI20 RE, UI20 GP, UI20 PW, UI20S DB, UI20S RE, UI20S PW,;, Ice Cooling IPL Hair Removal Device; Model(S): UIM20 GR, UIM20 BK, UIM20 SL, UIM20 CB, UIM20 WR, JMOON NouvelleSkin Facial Toning Device; Model(S): M30U PR, M30U MW, M30U SG, M30U SK, M30U MP and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Contract manufacturer, Exporter to the US | accessdata.fda.gov |
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Contract manufacturer, Exporter to the US | accessdata.fda.gov |
| Media, Electroconductive | GYB | 2 | Exporter to the US | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 2 | Contract manufacturer, Exporter to the US | accessdata.fda.gov |
| Stimulator, Transcutaneous Electrical, Aesthetic Purposes | NFO | 2 | Contract manufacturer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 8, 2025 | K243749 | Jmoon Conductive Gel | GYB | Substantially Equivalent | Shenzhen Ulike Smart Electronics Co., Ltd. | accessdata.fda.gov |
| February 5, 2025 | K243555 | LED light therapy mask (E43, E32, E49B, E49C, E100B, E100C, E103B, E104B, E106A, E108A) | OLP | Substantially Equivalent | Shenzhen Eyco Technology Co., Ltd. | accessdata.fda.gov |
| November 6, 2024 | K242039 | Ice Cooling IPL Hair Removal Device (UIM20 GR, UIM20 BK, UIM20 SL, UIM20 CB, UIM20 WR) | OHT | Substantially Equivalent | Shenzhen Ulike Smart Electronics Co., Ltd. | accessdata.fda.gov |
| January 11, 2024 | K233664 | 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,) | OHT | Substantially Equivalent | Shenzhen Ulike Smart Electronics Co., Ltd. | accessdata.fda.gov |
| January 5, 2024 | K233679 | IPL 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) | OHT | Substantially Equivalent | Shenzhen Ulike Smart Electronics Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Media, Electroconductive
- All makers of Light Based Over The Counter Wrinkle Reduction
- All makers of Over-The-Counter Powered Light Based Laser For Acne
- All makers of Light Based Over-The-Counter Hair Removal
- All makers of Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Updated April 8, 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.