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Lodestar Products, Inc.

Country not established

Devices
1

What Lodestar Products, Inc. makes

Lodestar Products, Inc. manufactures skin barrier films designed to protect and maintain the integrity of the skin, commonly used in medical and post-operative care settings.

The company’s products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Skin Barrier Film Ref K092712

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

Frequently asked questions

How many devices does Lodestar Products, Inc. have in the registry?

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

Which registries list Lodestar Products, Inc.'s devices?

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

What risk classes do Lodestar Products, Inc.'s devices fall under?

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

What are the newest devices from Lodestar Products, Inc. in the registry?

The most recently registered devices listed for Lodestar Products, Inc. include SKIN BARRIER FILM.

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