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Ammerman Medical Enterprises, Inc.

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Devices
1

What Ammerman Medical Enterprises, Inc. makes

Ammerman Medical Enterprises, Inc. manufactures the AMPU-PAK, a device designed for the safe and sterile removal of amputated body parts, including fingers, toes, and limbs, to prevent contamination and preserve tissue integrity.

The AMPU-PAK is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company 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

  • Ampu-Pak Ref K860511

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

Frequently asked questions

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

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

Which registries list Ammerman Medical Enterprises, Inc.'s devices?

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

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

The most recently registered devices listed for Ammerman Medical Enterprises, Inc. include AMPU-PAK.

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