Asclepion Laser Technologies GmbH
Asclepion Laser Technologies GmbH holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2026.
Top product codes for Asclepion Laser Technologies GmbH
Recent clearances by Asclepion Laser Technologies GmbH
- K261094 — YellowStar
- K253100 — MultiPulse TFL
- K240831 — MultiCut Solo
- K241600 — Dermablate
- K240816 — MeDioStar
- K231876 — MultiPulse HoPLUS
- K213597 — MultiCut Solo
- K213889 — PicoStar
- K210634 — MCL 31 Dermablate System
- K192483 — MeDioStar
- K161257 — MultiPulse HoPLUS
- K152153 — MicroSpot Handpiece
- K150140 — MCL 31 Dermablate
- K143519 — The MeDioStar NeXT Family
- K133891 — MULTIPULSE TM+1470
- K131987 — MULTIPULSE HOPLUS
- K131757 — TATTOOSTAR EFFECT COMBO
- K133297 — QUADROSTARPROGREEN, QUADROSTARPROYELLOW
- K113489 — ORION
- K112669 — TATTOOSTAR EFFECT Y
- K111851 — MEDIOSTAR NEXT
- K081541 — DERMABLATE EFFECT
- K071451 — TATTOOSTAR Y
- K060787 — TATTOOSTAR FAMILY
- K060455 — MULTISTAR
- K060457 — QUADROSTAR 532
- K060459 — QUADROSTAR 980
- K050900 — MEDIOSTAR XT
- K042968 — MCL 30 DERMABLATE ER:YAG LASER SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.