Tivic Health Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tivic Health Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ClearUP Sinus Pain Relief
2
Total
1
Cleared
1
Denied
Tivic Health Systems, Inc. has 1 FDA 510(k) cleared medical devices. Based in Menlo Park, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Tivic Health Systems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medical Device Regulatory Consultant as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Tivic Health Systems, Inc.
2 devices