Somnetics International, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Somnetics International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Transcend 365 miniCPAP System
3
Total
3
Cleared
0
Denied
Somnetics International, Inc. has 3 FDA 510(k) cleared medical devices. Based in New Brighton, US.
Historical record: 3 cleared submissions from 2013 to 2018. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Somnetics International, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bluebird Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Somnetics International, Inc.
3 devices