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Prins Medical Ind., Inc.

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Devices
1

What Prins Medical Ind., Inc. makes

Prins Medical Ind., Inc. manufactures the PORT-A-POLE, a medical device designed for securing intravenous (IV) lines to patients’ extremities, reducing the risk of dislodgement or accidental removal.

The PORT-A-POLE is classified as a Class I device under FDA regulations and is listed via the 510(k) pathway. 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

  • Port-A-Pole Ref K961470

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

Frequently asked questions

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

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

Which registries list Prins Medical Ind., Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Prins Medical Ind., Inc. include PORT-A-POLE.

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