Cleared Traditional

Led Light Phototherapy Bed (Pro 450/ GY-680A)

K252786 · Shenzhen Suyzeko Limited. · General & Plastic Surgery
Dec 2025
Decision
90d
Days
Class 2
Risk

About This 510(k) Submission

K252786 is an FDA 510(k) clearance for the Led Light Phototherapy Bed (Pro 450/ GY-680A), a Fat Reducing Low Level Laser (Class II — Special Controls, product code OLI), submitted by Shenzhen Suyzeko Limited. (Shenzhen, CN). The FDA issued a Cleared decision on December 1, 2025, 90 days after receiving the submission on September 2, 2025. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.5400.

Submission Details

510(k) Number K252786 FDA.gov
FDA Decision Cleared SESE
Date Received September 02, 2025
Decision Date December 01, 2025
Days to Decision 90 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code OLI — Fat Reducing Low Level Laser
Device Class Class II — Special Controls
CFR Regulation 21 CFR 878.5400
Definition Non-invasive Reduction In Fat Layer For Body Contouring