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Acorn Medical, Inc.

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Devices
1

What Acorn Medical, Inc. makes

Acorn Medical, Inc. manufactures the INSUFO-GARD series (models #100-104), which are infusion pumps designed for controlled delivery of fluids in medical settings.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Insufo-Gard #100-104 Ref K930767

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

Frequently asked questions

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

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

Which registries list Acorn Medical, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Acorn Medical, Inc. include INSUFO-GARD #100-104.

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