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Big Sky Laser Technologies, Inc.

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Devices
1

What Big Sky Laser Technologies, Inc. makes

Big Sky Laser Technologies, Inc. manufactures the PROLITE Pulsed Light System, a device designed for medical and aesthetic treatments using pulsed light technology.

The PROLITE Pulsed Light System 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, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Prolite Pulsed Light System Ref K021304

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

Frequently asked questions

How many devices does Big Sky Laser Technologies, Inc. have in the registry?

The registry currently lists 1 device for Big Sky Laser Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Big Sky Laser Technologies, Inc.'s devices?

Among its 1 most recently registered device, Big Sky Laser Technologies, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Big Sky Laser Technologies, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Big Sky Laser Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Big Sky Laser Technologies, Inc. in the registry?

The most recently registered devices listed for Big Sky Laser Technologies, Inc. include PROLITE PULSED LIGHT SYSTEM.

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