Mlay T11A
by Shenzhen Mlay Intelligent Technology Co., Ltd. 4 variants
Mlay T11A is a home-use intense pulsed light hair removal unit (FDA Class II; FDA product code OHT, Light Based Over-The-Counter Hair Removal) made by Shenzhen Mlay Intelligent Technology Co., Ltd., cleared under FDA 510(k) K240264 on 8 Mar 2024 and listed in FDA GUDID since 20 Jul 2026 (UDI-DI 06977357490171), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06977357490171 | Date20 Jul 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK240264 | Date8 Mar 2024 | StatusActive |
Official records
- AccessGUDID record 06977357490171
- FDA 510(k) database K240264
Across registries
- FDA 510(k) K240264 decided 8 Mar 2024 Active
- FDA GUDID UDI-DI 06977357490171 listed 20 Jul 2026 Listed
Timeline
- Cleared FDA 510(k) K240264
- Listed FDA GUDID 06977357490171
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Mlay
- Generic name
- Home-use intense pulsed light hair removal unit
- Model / reference
- T11A
- Primary DI / UDI-DI
- 06977357490171
- 510(k) Number
- FDA product code
- OHT
- GMDN term
- Home-use intense pulsed light hair removal unit
- Device class
- Class II
- Regulation number
- 878.4810
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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- Hand-held IPL device (JOVS Hair Removal Device) by Shenzhen Qianyu Technology Co., Ltd.
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- NUBRILLIANCE PULSED LIGHT HAIR REMOVAL DEVICE by Wellquest Intl., Inc.
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