Liquet Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Liquet Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Versus™ Catheter (VS110-9NB), Versus™ Catheter (VS110-8B)
2
Total
2
Cleared
0
Denied
Liquet Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Glen Allen, US.
Latest FDA clearance: Feb 2026. Active since 2024. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Liquet Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Evergreen Strategic Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Liquet Medical, Inc.
2 devices