Medical Device Manufacturer · US , Centercille , MA

Lokki Lasers Medicaux - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003

Total

Cleared

Denied

Lokki Lasers Medicaux has 1 FDA 510(k) cleared medical devices. Based in Centercille, US.

Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Lokki Lasers Medicaux Filter by specialty or product code using the sidebar.

Lokki Lasers Medicaux is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Lokki Lasers Medicaux

1 devices

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