Insera Therapeutics, Inc. is one of 16353 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Insera Therapeutics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CLEAR™ Aspiration System
1
Total
1
Cleared
0
Denied
Insera Therapeutics, Inc. has 1 FDA 510(k) cleared medical devices. Based in Dallas, US.
Latest FDA clearance: Jun 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Insera Therapeutics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Insera Therapeutics, Inc.
1 devices