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Northfleet Management Group, Inc.

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Devices
1

What Northfleet Management Group, Inc. makes

Northfleet Management Group, Inc. manufactures the MANGAR BOOSTER, a medical device designed to enhance or assist in specific clinical procedures or treatments.

The MANGAR BOOSTER is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Mangar Booster Ref K905414

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

Frequently asked questions

How many devices does Northfleet Management Group, Inc. have in the registry?

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

Which registries list Northfleet Management Group, Inc.'s devices?

Among its 1 most recently registered device, Northfleet Management Group, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Northfleet Management Group, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Northfleet Management Group, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Northfleet Management Group, Inc. in the registry?

The most recently registered devices listed for Northfleet Management Group, Inc. include MANGAR BOOSTER.

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