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American Healthcare Products, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 1000099913

Devices
2
Registrations
FDA
FDA recalls
1

What American Healthcare Products, Inc. makes

American Healthcare Products, Inc. manufactures medical devices including PRN Thermalcare Model 3000 thermal therapy units and low protein, powder-free Uniseal gloves.

The company is based in the United States, and its portfolio includes Class I and Class II medical devices that are listed in the FDA 510(k) registry.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

Company details

FDA FEI number
1000099913
Address
1028 WESTMINSTER AVE., ALHAMBRA, CA, 91803

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

FDA recall records list 1 recall initiated by AMERICAN HEALTHCARE PRODUCTS, INC., initiated on 2002-07-23. By recorded status: 1 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

  • 2002

    • 23 Jul 2002 Z-0635-03 Unclassified (pre-2012) Terminated Unfit for intended use due to stickiness. Distribution: Nationwide. Submission number: K945164

Frequently asked questions

How many devices does AMERICAN HEALTHCARE PRODUCTS, INC. have in the registry?

The registry currently lists 2 devices for AMERICAN HEALTHCARE PRODUCTS, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list AMERICAN HEALTHCARE PRODUCTS, INC.'s devices?

Among its 2 most recently registered devices, AMERICAN HEALTHCARE PRODUCTS, INC. has devices listed in FDA 510(k) (2 devices).

What risk classes do AMERICAN HEALTHCARE PRODUCTS, INC.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for AMERICAN HEALTHCARE PRODUCTS, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for AMERICAN HEALTHCARE PRODUCTS, INC.?

FDA recall records list 1 recall initiated by AMERICAN HEALTHCARE PRODUCTS, INC., the most recent initiated on 23 Jul 2002. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from AMERICAN HEALTHCARE PRODUCTS, INC. in the registry?

The most recently registered devices listed for AMERICAN HEALTHCARE PRODUCTS, INC. include PRN THERMALCARE, MODEL 3000 and UNISEAL GLOVES (LOW PROTEIN, POWDER FREE).

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

This is an FDA establishment record. No EUDAMED registration is known for this company.