Prosomnus Sleep Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Prosomnus Sleep Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ProSomnus EVO Sleep and Snore Device, ProSomnus EVO Sleep and Snore Device with Patient Monitoring
1
Total
1
Cleared
0
Denied
Prosomnus Sleep Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Pleasanton, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Prosomnus Sleep Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Prosomnus Sleep Technologies, Inc.
1 devices