Cleared Traditional

K253279 - Feather/numiere 05 06 07 (05) (FDA 510(k) Clearance)

Dec 2025
Decision
86d
Days
Class 2
Risk

K253279 is an FDA 510(k) clearance for the Feather/numiere 05 06 07 (05). This device is classified as a Light Based Over The Counter Wrinkle Reduction (Class II - Special Controls, product code OHS).

Submitted by Heat IN A Click, LLC (Dania, US). The FDA issued a Cleared decision on December 24, 2025, 86 days after receiving the submission on September 29, 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 K253279 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 29, 2025
Decision Date December 24, 2025
Days to Decision 86 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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