Data / Medical devices / China / Shenzhen Mlay Intelligent Technology Co., Ltd.
Shenzhen Mlay Intelligent Technology Co., Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 4 510(k) clearances
Shenzhen Mlay Intelligent Technology Co., Ltd. is registered with the FDA (registration 3031182672) in Shenzhen Guangdong, China. It lists 1 device type. The FDA files 4 510(k) clearances under its listings, the newest dated February 23, 2026. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3031182672
- Address
- 201, 106-01, Building 28, Cuigang Industrial Zone 2, Huaide Community, Fuyong Street, Baoan District, Shenzhen Guangdong, China, 518000
- Owner or operator
- Shenzhen Mlay Intelligent Technology Co.,Ltd. (10089650)
- Roles
- Manufacturer
- First device listed
- March 15, 2024
- Registered through
- 2026
- Brand names listed
- Amifiy IPL Hair Removal Device (Model: T18B), Amifiy Ice Cooling IPL Home Use Hair Removal Device(Model:T18A), CBG Devices Ice Cooling IPL Home Use Hair Removal Devices (Model: T10B), DUDEPRUNER Fuzz Gun Pro (Model: FGP), Danrah Ice Cooling IPL Home Use Hair Removal Device(Model:T16A), Dreame Astra IPL Hair Removal Device, IPL Hair Removal Device (Model(s): T14B, T16B, T19B, T15B, T17C, T18B, T21A, T21B, T21C, T21D, T22A, T22B, T25B, T25C), IPL Hair Removal Device (Models: T31A, T32A) and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Light Based Over-The-Counter Hair Removal | OHT | 2 | 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 |
|---|---|---|---|---|---|---|
| February 23, 2026 | K253666 | IPL Hair Removal Device (Models: T31A, T32A) | OHT | Substantially Equivalent | Shenzhen Mlay Intelligent Technology Co., Ltd. | accessdata.fda.gov |
| August 14, 2025 | K251176 | IPL Hair Removal Device (Model(s): T14B, T16B, T19B, T15B, T17C, T18B, T21A, T21B, T21C, T21D, T22A, T22B, T25B, T25C) | OHT | Substantially Equivalent | Shenzhen Mlay Intelligent Technology Co., , Ltd. | accessdata.fda.gov |
| May 22, 2024 | K241106 | Ice Cooling IPL Home Use Hair Removal Device (Model(s): T10B, T10C, T15A, T17A, T18A, T14A, T16A, T19A) | OHT | Substantially Equivalent | Shenzhen Mlay Intelligent Technology Co., , Ltd. | accessdata.fda.gov |
| March 8, 2024 | K240264 | Home Use Hair Removal Device (Model(s):T10A, T10B, T10C, T10D, T11A, T15A, T17A, T18A, T14A, T16A, T19A) | OHT | Substantially Equivalent | Shenzhen Mlay Intelligent Technology Co., , Ltd. | accessdata.fda.gov |
Compare with other makers
Updated February 23, 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.