Xhale, Inc. is one of 18366 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Xhale, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Nasal Alar SpO2 Sensor, Assurance Alar / Nasal SpO2 Sensor
2
Total
2
Cleared
0
Denied
Xhale, Inc. has 2 FDA 510(k) cleared medical devices. Based in Gainesville, US.
Historical record: 2 cleared submissions from 2015 to 2017. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Xhale, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Xhale, Inc. C/O Promedic, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Xhale, Inc.
2 devices