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

LumiGlam Laser System (SHE-LSP601-3)

K Number: K260690 · Decision Jun 4, 2026
Classifications
1
FEI Numbers
478
Registration Numbers
480
Same Product Code
2867
Applicant Total
6
Review Days
93

Basic Information

Device Name
LumiGlam Laser System (SHE-LSP601-3)
K Number
K260690
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
Beijing Sano Laser S&T Development Co.,Ltd
Date Received
March 3, 2026
Decision Date
June 4, 2026
Product Code
GEX
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
GEX Powered Laser Surgical Instrument

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