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Harding Industries, Inc.

United StatesFDA applicant, unverified

Devices
2

What Harding Industries, Inc. makes

Harding Industries, Inc. manufactures a Shave Prep Kit, used for preparing skin prior to surgical procedures, and nasopharyngeal airways, which are inserted through the nose to maintain an open airway in patients requiring respiratory support.

The company’s products are regulated under FDA Class I and Class II designations, with some devices requiring 510(k) clearance. The manufacturer 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

  • Shave Prep Kit Ref K945481

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Nasopharyngeal Airway Ref K871673

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

Frequently asked questions

How many devices does Harding Industries, Inc. have in the registry?

The registry currently lists 2 devices for Harding Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Harding Industries, Inc.'s devices?

Among its 2 most recently registered devices, Harding Industries, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Harding Industries, Inc.'s devices fall under?

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

What are the newest devices from Harding Industries, Inc. in the registry?

The most recently registered devices listed for Harding Industries, Inc. include SHAVE PREP KIT and NASOPHARYNGEAL AIRWAY.

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