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Nagle Co.

Country not established

Devices
1

What Nagle Co. makes

Nagle Co. manufactures the NALGENE Emergency Eye Wash, a Class I device designed for flushing eyes in response to chemical or foreign-body exposure to reduce injury risk.

The device is regulated under FDA’s 510(k) pathway as a Class I product and is listed in the FDA’s 510(k) database. 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

  • Nalgene Emergency Eye Wash Ref K760820

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

Frequently asked questions

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

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

Which registries list Nagle Co.'s devices?

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

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

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

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

The most recently registered devices listed for Nagle Co. include NALGENE EMERGENCY EYE WASH.

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