Cleared Traditional

K252603 - HIGHERDOSE Body Sculptor (Model: GS-03) (FDA 510(k) Clearance)

Jan 2026
Decision
163d
Days
Class 2
Risk

K252603 is an FDA 510(k) clearance for the HIGHERDOSE Body Sculptor (Model: GS-03). This device is classified as a Light Based Over The Counter Wrinkle Reduction (Class II - Special Controls, product code OHS).

Submitted by Shenzhen Kaiyan Medical Equipment Co., Ltd. (Shenzhen, CN). The FDA issued a Cleared decision on January 28, 2026, 163 days after receiving the submission on August 18, 2025.

This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4810. Use Of Light Based Treatment To Reduce Wrinkles On The Body In General Or Specific Anatomical Locations Depending On The Information Provided..

Submission Details

510(k) Number K252603 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 18, 2025
Decision Date January 28, 2026
Days to Decision 163 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code OHS — Light Based Over The Counter Wrinkle Reduction
Device Class Class II - Special Controls
CFR Regulation 21 CFR 878.4810
Definition Use Of Light Based Treatment To Reduce Wrinkles On The Body In General Or Specific Anatomical Locations Depending On The Information Provided.

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