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Molloy Corp.

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Devices
1

What Molloy Corp. makes

Molloy Corp. manufactures the Molloy Intubating Stylette, a medical device designed to assist in the insertion of endotracheal tubes during intubation procedures.

The device is classified as Class I under FDA regulations and is listed in the FDA’s 510(k) clearance registry. 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

  • Molloy Intubating Stylette Ref K943104

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

Frequently asked questions

How many devices does Molloy Corp. have in the registry?

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

Which registries list Molloy Corp.'s devices?

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

What risk classes do Molloy Corp.'s devices fall under?

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

What are the newest devices from Molloy Corp. in the registry?

The most recently registered devices listed for Molloy Corp. include MOLLOY INTUBATING STYLETTE.

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