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# FDA Clears ReddyPort Ventilation Device
- URL: https://www.fdaweb.com/fda-clears-reddyport-ventilation-device/
- Published: 2023-07-19T12:00:00.000Z
- Updated: 2026-09-14T18:45:08.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5154909

FDA has given 510(k) clearance to the ReddyPort elbow device used in non-invasive ventilation. A company [statement](https://www.prnewswire.com/news-releases/fda-clears-reddyport-non-invasive-ventilation-device-301879694.html?ref=fdaweb.com) says the elbow features a self-sealing valve that provides seamless oral access to the patient’s mouth without the need for mask removal, alleviating the risk of therapeutic pressure loss and maintaining lung compliance.

The company says non-invasive ventilation is the first line of therapy in respiratory insufficiency or failure commonly seen with chronic obstructive pulmonary disease, congestive heart failure, asthma, pneumonia, or acute respiratory distress syndrome.