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Medical Resources International, Inc.

United StatesFDA applicant, unverified

Devices
2

What Medical Resources International, Inc. makes

Medical Resources International, Inc. manufactures protective barriers, including the ULTRA SHIELD PF and ULTAR-SHIELD, designed for use in medical environments to prevent contamination and cross-transmission of pathogens.

These products are classified as Class I devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Ultra Shield Pf Ref K934171

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Ultar-Shield Ref K932702

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

Frequently asked questions

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

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

Which registries list Medical Resources International, Inc.'s devices?

Among its 2 most recently registered devices, Medical Resources International, Inc. has devices listed in FDA 510(k) (2 devices).

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

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

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

The most recently registered devices listed for Medical Resources International, Inc. include ULTRA SHIELD PF and ULTAR-SHIELD.

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