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Integra Luxtec, Inc.

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Devices
1

What Integra Luxtec, Inc. makes

Integra Luxtec, Inc. manufactures the LUXTEC MLX LIGHT SOURCE, a medical device designed for photodynamic therapy applications in surgical settings. This device emits controlled light at specific wavelengths to activate photosensitizing agents, aiding in tissue treatment or removal procedures.

The LUXTEC MLX LIGHT SOURCE is classified as a Class II device under FDA regulations and has undergone 510(k) clearance. The company is based in the United States, and its device is listed in the FDA’s 510(k) registry.

AI-generated from registry data, 19 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Luxtec Mlx Light Source Ref K081477

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

Frequently asked questions

How many devices does Integra Luxtec, Inc. have in the registry?

The registry currently lists 1 device for Integra Luxtec, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Integra Luxtec, Inc.'s devices?

Among its 1 most recently registered device, Integra Luxtec, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Integra Luxtec, Inc.'s devices fall under?

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

What are the newest devices from Integra Luxtec, Inc. in the registry?

The most recently registered devices listed for Integra Luxtec, Inc. include LUXTEC MLX LIGHT SOURCE.

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