LED Light Therapy Mask (Models: T2, RLD10)— 510(k) K254079
Substantially EquivalentShenzhen Desida Technology Co., Ltd.
FDA 510(k) clearance K254079 for LED Light Therapy Mask (Models: T2, RLD10), Substantially Equivalent on 2026-03-16. Applicant: Shenzhen Desida Technology Co., Ltd.. Device class: 2.
Summary
Shenzhen Desida Technology's LED Light Therapy Mask is filed under OHS, light-based over-the-counter wrinkle reduction. The name lists two models, T2 and RLD10.
Class II, 21 CFR 878.4810. It was a Traditional 510(k), and General and Plastic Surgery is both the classification panel and the review panel.
Shenzhen Desida Technology filed from Shenzhen, China. The decision came 88 calendar days after FDA received it (December 18, 2025 to March 16, 2026).
Clearance details
- Applicant
- Shenzhen Desida Technology Co., Ltd.
- Product code
- Product code OHS
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
Recent devices under product code OHS
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view all- K251450 — Baby Nasal Aspirator (5 models)
- K244033 — Electric Nasal Aspirator (NASA601,NASA602,NASA603,NASA605,NASA606,NASA608,NASA610)
- K233901 — Baby Nasal Aspirator (KA1006, KA1001, KA1005, NASA005, NASA006, NASA008, NASA009)
- K221643 — Hair Removal Device (Model: IPL-D26, IPL-D19)
- K221635 — IPL sapphire ice cooling hair remove device
Adverse events under product code OHS
product code OHS- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.