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

MOSES Raydar™

K Number: K260100 · Decision May 18, 2026
Classifications
1
FEI Numbers
478
Registration Numbers
480
Same Product Code
2867
Applicant Total
231
Review Days
125

Basic Information

Device Name
MOSES Raydar™
K Number
K260100
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
Boston Scientific Corporation
Date Received
January 13, 2026
Decision Date
May 18, 2026
Product Code
GEX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
GU
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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