Medical Device Manufacturer · US , Chelmsford , MA

Asclepion Laser Technologies GmbH - FDA 510(k) Cleared Devices

29 submissions · 29 cleared · Since 2004

Recent clearances: YellowStar, MultiPulse TFL, MultiCut Solo

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29
Total
29
Cleared
0
Denied

FDA 510(k) Regulatory Record - Asclepion Laser Technologies GmbH General & Plastic Surgery ✕

27 devices
1-12 of 27
Cleared Apr 29, 2026
YellowStar
K261094 · GEX
General & Plastic Surgery · 27d
Cleared Oct 23, 2025
MultiPulse TFL
K253100 · GEX
General & Plastic Surgery · 29d
Cleared Jul 03, 2024
Dermablate
K241600 · GEX
General & Plastic Surgery · 29d
Cleared Apr 23, 2024
MeDioStar
K240816 · GEX
General & Plastic Surgery · 29d
Cleared Feb 22, 2024
MultiPulse HoPLUS
K231876 · GEX
General & Plastic Surgery · 241d
Cleared Apr 22, 2022
PicoStar
K213889 · GEX
General & Plastic Surgery · 130d
Cleared Apr 13, 2022
MCL 31 Dermablate System
K210634 · GEX
General & Plastic Surgery · 406d
Cleared Mar 13, 2020
MeDioStar
K192483 · GEX
General & Plastic Surgery · 185d
Cleared Mar 31, 2017
MultiPulse HoPLUS
K161257 · GEX
General & Plastic Surgery · 331d
Cleared Dec 11, 2015
MicroSpot Handpiece
K152153 · GEX
General & Plastic Surgery · 130d
Cleared Jun 05, 2015
MCL 31 Dermablate
K150140 · GEX
General & Plastic Surgery · 134d
Cleared Mar 10, 2015
The MeDioStar NeXT Family
K143519 · GEX
General & Plastic Surgery · 88d
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