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Lerner Medical Devices, Inc.

United StatesFDA applicant, unverified

Devices
3

What Lerner Medical Devices, Inc. makes

Lerner Medical Devices, Inc. manufactures phototherapy systems, including the LH-75, LH-75T, and Levia models, designed for medical light-based treatments.

These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.

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

Catalogue3

Newest first, rows 1-3 of 3

  • Lh-75 Phototherapy System Ref K091568

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Lh-75T Phototherapy System Ref K090097

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Levia Phototherapy System Ref K040062

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

Frequently asked questions

How many devices does Lerner Medical Devices, Inc. have in the registry?

The registry currently lists 3 devices for Lerner Medical Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Lerner Medical Devices, Inc.'s devices?

Among its 3 most recently registered devices, Lerner Medical Devices, Inc. has devices listed in FDA 510(k) (3 devices).

What risk classes do Lerner Medical Devices, Inc.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Lerner Medical Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Lerner Medical Devices, Inc. in the registry?

The most recently registered devices listed for Lerner Medical Devices, Inc. include LH-75 PHOTOTHERAPY SYSTEM, LH-75T PHOTOTHERAPY SYSTEM and LEVIA PHOTOTHERAPY SYSTEM.

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