K251176 is an FDA 510(k) clearance for the IPL Hair Removal Device (Model(s): T14B, T16B, T19B, T15B, T17C, T18B, T21A, .... Classified as Light Based Over-the-counter Hair Removal (product code OHT), Class II - Special Controls.
Submitted by Shenzhen Mlay Intelligent Technology Co., Ltd. (Shenzhen, CN). The FDA issued a Cleared decision on August 14, 2025 after a review of 120 days - within the typical 510(k) review window.
This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4810 - the FDA general and plastic surgery device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.
Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.
View all Shenzhen Mlay Intelligent Technology Co., Ltd. devices