Trisalus Life Sciences is one of 16090 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Trisalus Life Sciences - FDA 510(k) Cleared Devices
Recent clearances: TriSalus TriNav Advance Infusion System, TriSalus TriGuideTM Guiding Catheter, TriSalus TriNav® LV Infusion System
4
Total
4
Cleared
0
Denied
Trisalus Life Sciences has 4 FDA 510(k) cleared medical devices. Based in Westminster, US.
Latest FDA clearance: Sep 2026. Active since 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Trisalus Life Sciences Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Trisalus Life Sciences
4 devices