Cleared Traditional

K253874 - LED Therapy Light (COB1400, HP1800PRO) (FDA 510(k) Clearance)

Mar 2026
Decision
89d
Days
Class 2
Risk

K253874 is an FDA 510(k) clearance for the LED Therapy Light (COB1400, HP1800PRO). This device is classified as a Light Based Over The Counter Wrinkle Reduction (Class II - Special Controls, product code OHS).

Submitted by Shenzhen Hanhua Opto Co., Ltd. (Shenzhen, CN). The FDA issued a Cleared decision on March 3, 2026, 89 days after receiving the submission on December 4, 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 K253874 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 04, 2025
Decision Date March 03, 2026
Days to Decision 89 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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