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Sheridan Catheter Corp.

United StatesFDA applicant, unverified

Devices
39

What Sheridan Catheter Corp. makes

Sheridan Catheter Corp. manufactures airway management devices, including endotracheal tubes, laser-compatible tracheal tubes, and tracheobronchial suction catheters. Their portfolio also covers naso-intestinal feeding tubes, differential ventilation tubes, and accessories like electrosurgery protection filters. Clinical electronic thermometers and topical anesthesia applicators for the larynx/trachea are additional offerings.

The company’s devices are classified under FDA’s Class I and Class II categories, with most submissions recorded via the 510(k) pathway. Products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.

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

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Frequently asked questions

How many devices does Sheridan Catheter Corp. have in the registry?

The registry currently lists 39 devices for Sheridan Catheter Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Sheridan Catheter Corp.'s devices?

Among its 39 most recently registered devices, Sheridan Catheter Corp. has devices listed in FDA 510(k) (39 devices).

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

Among its 39 most recently registered devices, the classes recorded for Sheridan Catheter Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Sheridan Catheter Corp. in the registry?

The most recently registered devices listed for Sheridan Catheter Corp. include ENDOTRACHEAL TUBE, ACCESSORY, LAZER-TRACH TRACHEAL TUBE, INTRODUCTION/DRAINAGE CATHETER & ACCESS and CLINICAL ELECTRONIC THERMOMETERS.

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