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Dr. K. Honle GmbH

Country not established

Devices
3

What Dr. K. Honle GmbH makes

Dr. K. Honle GmbH manufactures ultraviolet (UV) light sources and diagnostic devices used in dermatology, including handheld UV lamps for skin examination and treatment assessment. The DERMALIGHT BLUE-POINT, UVASTAR 400, and SPOT models are designed to detect and analyze skin conditions under specific UV wavelengths, aiding in the identification of abnormalities such as fungal infections or pigmentation disorders.

These devices are classified under the FDA’s 510(k) premarket notification process, reflecting their status as Class II medical devices. The portfolio is regulated in the United States, where the company is based.

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

Catalogue3

Newest first, rows 1-3 of 3

  • Dermalight Blue-Point Ref K828674

    Not classified
    Active 510(k) 510(k) —

  • Dermalight Uvastar 400 Ref K828675

    Not classified
    Active 510(k) 510(k) —

  • Dermalight Spot Ref K828676

    Not classified
    Active 510(k) 510(k) —

Frequently asked questions

How many devices does Dr. K. Honle GmbH have in the registry?

The registry currently lists 3 devices for Dr. K. Honle GmbH. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dr. K. Honle GmbH's devices?

Among its 3 most recently registered devices, Dr. K. Honle GmbH has devices listed in FDA 510(k) (3 devices).

What are the newest devices from Dr. K. Honle GmbH in the registry?

The most recently registered devices listed for Dr. K. Honle GmbH include DERMALIGHT BLUE-POINT, DERMALIGHT UVASTAR 400 and DERMALIGHT SPOT.

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