FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

LED Light Therapy Mask (K9C-TK, K9C-K, K9P-YK, K9P-K, FM-03BK, FM-09K)

K Number: K260946 · Decision Jun 18, 2026
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
152
Applicant Total
3
Review Days
87

Basic Information

Device Name
LED Light Therapy Mask (K9C-TK, K9C-K, K9P-YK, K9P-K, FM-03BK, FM-09K)
K Number
K260946
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Guangdong Newdermo Biotech Co., Ltd.
Date Received
March 23, 2026
Decision Date
June 18, 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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OHS), ordered by most recent decision date.

View all

Other Clearances by Guangdong Newdermo Biotech Co., Ltd.

K Number Device Name
K260202 LED Light Therapy Masks (LumiLips FAC07NA)
K223544 LED light therapy mask (FM-01, FM-02, FM-03)