Asclepion Laser Technologies GmbH

FDA Regulatory Profile

Asclepion Laser Technologies GmbH appears in FDA public data with 0 recalls, 29 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Apr 29, 2026.

Summary

Total Recalls
0
510(k) Clearances
29
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K261094YellowStarApr 29, 2026
K253100MultiPulse TFLOct 23, 2025
K240831MultiCut SoloNov 6, 2024
K241600DermablateJul 3, 2024
K240816MeDioStarApr 23, 2024
K231876MultiPulse HoPLUSFeb 22, 2024
K213597MultiCut SoloJan 18, 2023
K213889PicoStarApr 22, 2022
K210634MCL 31 Dermablate SystemApr 13, 2022
K192483MeDioStarMar 13, 2020
K161257MultiPulse HoPLUSMar 31, 2017
K152153MicroSpot HandpieceDec 11, 2015
K150140MCL 31 DermablateJun 5, 2015
K143519The MeDioStar NeXT FamilyMar 10, 2015
K133891MULTIPULSE TM+1470Jan 30, 2015
K131987MULTIPULSE HOPLUSOct 15, 2014
K131757TATTOOSTAR EFFECT COMBOJul 17, 2014
K133297QUADROSTARPROGREEN, QUADROSTARPROYELLOWJun 10, 2014
K113489ORIONJul 27, 2012
K112669TATTOOSTAR EFFECT YMay 11, 2012