FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

YellowStar

K Number: K261094 · Decision Apr 29, 2026
Classifications
1
FEI Numbers
478
Registration Numbers
480
Same Product Code
2867
Applicant Total
29
Review Days
27

Basic Information

Device Name
YellowStar
K Number
K261094
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Asclepion Laser Technologies GmbH
Date Received
April 2, 2026
Decision Date
April 29, 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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K213597 MultiCut Solo
K213889 PicoStar
K210634 MCL 31 Dermablate System
K192483 MeDioStar
K161257 MultiPulse HoPLUS
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