FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

FAQ™ (LED Panel); FAQ™ (Dual LED Panel)

K Number: K253683 · Decision Feb 20, 2026
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
152
Applicant Total
10
Review Days
91

Basic Information

Device Name
FAQ™ (LED Panel); FAQ™ (Dual LED Panel)
K Number
K253683
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Foreo, Inc.
Date Received
November 21, 2025
Decision Date
February 20, 2026
Product Code
OHS
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OHS Light Based Over The Counter Wrinkle Reduction

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