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Nozees Co.

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Devices
1

What Nozees Co. makes

Nozees Co. makes the Nozees Nostril Dilator, a device designed to widen the nasal passages for improved airflow.

The Nozees Nostril Dilator is classified as a Class I medical device and is listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Nozees Nostril Dilator Ref K862406

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

Frequently asked questions

How many devices does Nozees Co. have in the registry?

The registry currently lists 1 device for Nozees Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Nozees Co.'s devices?

Among its 1 most recently registered device, Nozees Co. has devices listed in FDA 510(k) (1 device).

What risk classes do Nozees Co.'s devices fall under?

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

What are the newest devices from Nozees Co. in the registry?

The most recently registered devices listed for Nozees Co. include NOZEES NOSTRIL DILATOR.

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