A.R.C Laser GmbH - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
A.R.C Laser GmbH has 6 FDA 510(k) cleared medical devices. Based in Rockville, US.
Last cleared in 2022. Active since 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by A.R.C Laser GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by A.R.C Laser GmbH
6 devices
Cleared
Sep 01, 2022
FOX 810, FOX 980
General & Plastic Surgery
189d
Cleared
Mar 17, 2020
Wolf445nm
General & Plastic Surgery
208d
Cleared
Sep 27, 2017
Cetus system, Cetus probe
Ophthalmic
247d
Cleared
Aug 16, 2016
A.R.C. Laser Surgical Fibers and Probes
General & Plastic Surgery
88d
Cleared
Aug 13, 2009
FOXQ 980 LASER
General & Plastic Surgery
121d
Cleared
Feb 22, 2008
FOX 1-980, FOX Q-1064, FOX-Q-810
General & Plastic Surgery
88d