Somnice, Inc. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Somnice, Inc. - FDA 510(k) Cleared Devices
Recent clearances: The iNAP One Sleep Therapy System
1
Total
1
Cleared
0
Denied
Somnice, Inc. has 1 FDA 510(k) cleared medical devices. Based in Hsinchu County, TW.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Somnice, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Maxis, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Somnice, Inc.
1 devices