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Nutec Med, Inc.

Country not established

Devices
1

What Nutec Med, Inc. makes

Nutec Med, Inc. manufactures pressure-quiet tourniquets, designed for use in medical settings to control venous and arterial blood flow during procedures.

The company’s products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Pressure-Quet Tourniquet Ref K822553

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

Frequently asked questions

How many devices does Nutec Med, Inc. have in the registry?

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

Which registries list Nutec Med, Inc.'s devices?

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

What risk classes do Nutec Med, Inc.'s devices fall under?

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

What are the newest devices from Nutec Med, Inc. in the registry?

The most recently registered devices listed for Nutec Med, Inc. include PRESSURE-QUET TOURNIQUET.

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