Medical Device Manufacturer · US , Chelmsford , MA

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

28 submissions · 28 cleared · Since 2004
28
Total
28
Cleared
0
Denied

FDA 510(k) cleared devices by Asclepion Laser Technologies GmbH General & Plastic Surgery ✕

26 devices
1-12 of 26
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
Cleared Jan 30, 2015
MULTIPULSE TM+1470
K133891 · GEX
General & Plastic Surgery · 406d
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