Is this your brand? Sign in to claim ownership.

A.R.C. Laser GmbH

Germany·DE-MF-000009383

Last updated September 17, 2026

Information

Device	Model / Reference	Registries	Class	Status
Q-Las	LS09002-DVYS	EUDAMED	Class IIb	Active
Fox 810, Fox 980	K220531	FDA 510(k)	Class II	Active
Wolf445nm	K192272	FDA 510(k)	Class II	Active
Fox 1-980, Fox Q-1064, Fox-Q-810	K073322	FDA 510(k)	Class II	Active
Foxq 980 Laser	K091059	FDA 510(k)	Class II	Active
A.R.C. Laser Surgical Fibers and Probes	K161403	FDA 510(k)	Class II	Active
Cetus system, Cetus probe	K170183	FDA 510(k)	Class II	Active
Fox Iv	LS03500-AABB	EUDAMED	Class IIb	Active
Fox Iv	LS03500-BWAA	EUDAMED	Class IIb	Active
Fox Iv	LS03500-BWAB	EUDAMED	Class IIb	Active
Q-Las	LS09002-LLZS	EUDAMED	Class IIb	Active
Fox Iv	LS03500-GWAA	EUDAMED	Class IIb	Active
Cito 532	LS09010-S	EUDAMED	Class IIb	Active
Cobra	LS09011-DS	EUDAMED	Class IIb	Active
Fox Iv	LS03500-AWAB	EUDAMED	Class IIb	Active
Q-Las	LS09002-DVZS	EUDAMED	Class IIb	Active

No authorised representatives on record.

Not available yet.

Not available yet.

Not available yet.

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Jun 6, 2003	Z-0981-03	—	terminated	Product may not have been properly sterilized.

Establishments registered with the FDA under this company group, matched by name.