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Trans Texas Medical Devices Corp.

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Devices
1

What Trans Texas Medical Devices Corp. makes

Trans Texas Medical Devices Corp. manufactures the PRI A PUS, a medical device designed for the aspiration of pleural fluid or pus from the pleural space, commonly used in the treatment of pleural effusion or empyema.

The PRI A PUS is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. 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

  • Pri A Pus Ref K832756

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

Frequently asked questions

How many devices does Trans Texas Medical Devices Corp. have in the registry?

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

Which registries list Trans Texas Medical Devices Corp.'s devices?

Among its 1 most recently registered device, Trans Texas Medical Devices Corp. has devices listed in FDA 510(k) (1 device).

What risk classes do Trans Texas Medical Devices Corp.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Trans Texas Medical Devices Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Trans Texas Medical Devices Corp. in the registry?

The most recently registered devices listed for Trans Texas Medical Devices Corp. include PRI A PUS.

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