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La Lumiere, LLC

United StatesFDA applicant, unverified

Devices
2

What La Lumiere, LLC makes

La Lumiere, LLC manufactures over-the-counter (OTC) skincare devices, including the PRO X OTC 5—a handheld light therapy unit—and the ILLUMASK Acne Light Therapy Mask, designed for targeted skin treatment at home.

These devices fall under FDA Class II regulation and are listed via the 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.

Catalogue2

Newest first, rows 1-2 of 2

  • Pro X Otc 5 Ref K140471

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Illumask Acne Light Therapy Mask Ref K123999

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

Frequently asked questions

How many devices does La Lumiere, LLC have in the registry?

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

Which registries list La Lumiere, LLC's devices?

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

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

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

What are the newest devices from La Lumiere, LLC in the registry?

The most recently registered devices listed for La Lumiere, LLC include PRO X OTC 5 and ILLUMASK ACNE LIGHT THERAPY MASK.

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