Asclepion Laser Technologies GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
28
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253100MultiPulse TFLOctober 23, 2025
K240831MultiCut SoloNovember 6, 2024
K241600DermablateJuly 3, 2024
K240816MeDioStarApril 23, 2024
K231876MultiPulse HoPLUSFebruary 22, 2024
K213597MultiCut SoloJanuary 18, 2023
K213889PicoStarApril 22, 2022
K210634MCL 31 Dermablate SystemApril 13, 2022
K192483MeDioStarMarch 13, 2020
K161257MultiPulse HoPLUSMarch 31, 2017
K152153MicroSpot HandpieceDecember 11, 2015
K150140MCL 31 DermablateJune 5, 2015
K143519The MeDioStar NeXT FamilyMarch 10, 2015
K133891MULTIPULSE TM+1470January 30, 2015
K131987MULTIPULSE HOPLUSOctober 15, 2014
K131757TATTOOSTAR EFFECT COMBOJuly 17, 2014
K133297QUADROSTARPROGREEN, QUADROSTARPROYELLOWJune 10, 2014
K113489ORIONJuly 27, 2012
K112669TATTOOSTAR EFFECT YMay 11, 2012
K111851MEDIOSTAR NEXTJuly 8, 2011