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Laserlite, LLC

United StatesFDA applicant, unverified

Devices
2

What Laserlite, LLC makes

Laserlite, LLC manufactures diode lasers for surgical and medical applications, including the FeatherLite Diode Laser and the LaserLite Diode Surgical Laser. These devices are designed for precision cutting, coagulation, and tissue ablation in clinical settings.

The company’s portfolio is regulated under FDA Class II devices and is listed via the 510(k) clearance process. The products are based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Featherlite Diode Laser Ref K980142

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Laserlite Diode Surgical Laser Ref K981090

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

Frequently asked questions

How many devices does Laserlite, LLC have in the registry?

The registry currently lists 2 devices for Laserlite, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Laserlite, LLC's devices?

Among its 2 most recently registered devices, Laserlite, LLC has devices listed in FDA 510(k) (2 devices).

What risk classes do Laserlite, LLC's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Laserlite, LLC's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Laserlite, LLC in the registry?

The most recently registered devices listed for Laserlite, LLC include FEATHERLITE DIODE LASER and LASERLITE DIODE SURGICAL LASER.

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