Company · US
Avantec Vascular Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 2003 to 2026. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jan 7, 2026 | K251207 | Sangria Thrombectomy System Avantec Vascular Corporation | QEW |
| Aug 28, 2017 | K170987 | Captus Vascular Retrieval System Avantec Vascular Corporation | MMX |
| Feb 4, 2004 | K032436 | DURAMAX .018 BILIARY STENT SYSTEM Avantec Vascular Corp. | FGE |
| Jul 9, 2003 | K030638 | DURAMAX .035 BILIARY STENT SYSTEM, MODELS DML0718-80, DML0718-135, DML0818-80, DML0818-135, DML0918-80, DML0918-135, DML Avantec Vascular Corp. | FGE |
| Apr 3, 2003 | K030062 | ADMIRAL .035 DILATATION CATHETER, MODELS ADL0720-80,ADL0720-135,ADL0820-80, ADL0820-135,ADL0920-80,ADL0920-135,ADL1020-0 Avantec Vascular Corp. | LIT |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||