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Lokki Lasers Medicaux

Country not established

Devices
1

What Lokki Lasers Medicaux makes

Lokki Lasers Medicaux manufactures the RMO Plasma Curing Light, a device designed for plasma treatment and curing applications in medical settings.

The RMO Plasma Curing Light is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Rmo Plasma Curing Light Ref K024374

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Lokki Lasers Medicaux have in the registry?

The registry currently lists 1 device for Lokki Lasers Medicaux. Devices recorded under merged duplicate company entries are counted once.

Which registries list Lokki Lasers Medicaux's devices?

Among its 1 most recently registered device, Lokki Lasers Medicaux has devices listed in FDA 510(k) (1 device).

What risk classes do Lokki Lasers Medicaux's devices fall under?

Among its 1 most recently registered device, the classes recorded for Lokki Lasers Medicaux's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Lokki Lasers Medicaux in the registry?

The most recently registered devices listed for Lokki Lasers Medicaux include RMO PLASMA CURING LIGHT.

Generated automatically from registry data and not verified by a human reviewer.