Asclepion Laser Technologies GmbH - FDA 510(k) Cleared Devices
28
Total
28
Cleared
0
Denied
Asclepion Laser Technologies GmbH has 28 FDA 510(k) cleared medical devices. Based in Chelmsford, US.
Latest FDA clearance: Oct 2025. Active since 2004.
Browse the FDA 510(k) cleared devices submitted by Asclepion Laser Technologies GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Asclepion Laser Technologies GmbH
8 devices
Cleared
Oct 23, 2025
MultiPulse TFL
General & Plastic Surgery
29d
Cleared
Nov 06, 2024
MultiCut Solo
Obstetrics & Gynecology
225d
Cleared
Jul 03, 2024
Dermablate
General & Plastic Surgery
29d
Cleared
Apr 23, 2024
MeDioStar
General & Plastic Surgery
29d
Cleared
Feb 22, 2024
MultiPulse HoPLUS
General & Plastic Surgery
241d
Cleared
Jan 18, 2023
MultiCut Solo
Obstetrics & Gynecology
432d
Cleared
Apr 22, 2022
PicoStar
General & Plastic Surgery
130d
Cleared
Apr 13, 2022
MCL 31 Dermablate System
General & Plastic Surgery
406d