Dental Device Guide
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Not currently registered with FDA under this name

Lokki Lasers Medicaux

Centercille, MA, United States. Named as applicant on 1 dental 510(k) clearance between 2003 and 2003. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
12003–2003
Markets registered in
1United States
Establishments
0—
2003: 1200020102020

510(k) clearances per year, 2000–2026

510(k) clearances

Clearances on which FDA names Lokki Lasers Medicaux as the applicant.

Decided510(k)DeviceDevice type
10 Mar 2003K024374RMO PLASMA CURING LIGHTEBZ Ultraviolet Activator for Polymerization

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.