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Empire Industries, Inc.

United StatesFDA applicant, unverified

Devices
3

What Empire Industries, Inc. makes

Empire Industries, Inc. manufactures enteral feeding pumps and enteral feeding containers designed for administering nutrients directly into the gastrointestinal tract. These devices are intended for clinical use in patients requiring alternative nutrition support when oral intake is insufficient.

The company’s products are regulated as Class II medical devices under FDA requirements, with authorisation supported through the 510(k) clearance process. These devices are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Enteral Feeding Pump Ref K851351

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Enteral Feeding Container Ref K852966

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Enteral Feeding Pump Ref K852965

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

Frequently asked questions

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

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

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

Among its 3 most recently registered devices, Empire Industries, Inc. has devices listed in FDA 510(k) (3 devices).

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

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

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

The most recently registered devices listed for Empire Industries, Inc. include ENTERAL FEEDING PUMP and ENTERAL FEEDING CONTAINER.

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