This page includes the latest FDA filings for Trisalus Life Sciences. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3010909876 |
| FEI Number | 3010909876 |
| Name | Surefire Medical, Inc. |
| Owner & Operator | TriSalus Life Sciences |
| Contact Address | 6272 W. 91st Avenue Westminster CO 80031 US |
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 6272 W 91st Ave Westminster, CO 80031 US |
| Establishment Type | Complaint File Establishment per 21 CFR 820.198 |
Device Company | Device | Date |
|---|---|---|
TriSalus Life Sciences | TriSalus Infusion System | 2019-12-03 |
Surefire Medical, Inc. [TriSalus Life Sciences] | TriNav Infusion System | 2018-07-18 |
Surefire Medical, Inc. [TriSalus Life Sciences] | Spark Infusion System | 2018-07-18 |
Surefire Medical, Inc. [TriSalus Life Sciences] | Flexion Guiding Catheter | 2018-07-18 |
Surefire Medical, Inc. [TriSalus Life Sciences] | SIS Adaptor | 2018-02-16 |
Surefire Medical, Inc. [TriSalus Life Sciences] | Surefire Guiding Catheter | 2014-10-13 |
Surefire Medical, Inc. [TriSalus Life Sciences] | Surefire Precision Infusion System | 2014-10-13 |
Surefire Medical, Inc. [TriSalus Life Sciences] | Surefire Infusion System | 2014-10-13 |