Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Avantec Vascular with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jan 7, 2026: Sangria™ Thrombectomy System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jan 7, 2026 | Sangria™ Thrombectomy SystemK251207 · QEW | 510(k) clearances |
| Aug 28, 2017 | Captus Vascular Retrieval SystemK170987 · MMX | 510(k) clearances |
| Feb 4, 2004 | DURAMAX .018 BILIARY STENT SYSTEMK032436 · FGE | 510(k) clearances |
| Jul 9, 2003 | DURAMAX .035 BILIARY STENT SYSTEM, MODELS DML0718-80, DML0718-135, DML0818-80, DML0818-135, DML0918-80, DML0918-135, DMLK030638 · FGE | 510(k) clearances |
| Apr 3, 2003 | ADMIRAL .035 DILATATION CATHETER, MODELS ADL0720-80,ADL0720-135,ADL0820-80, ADL0820-135,ADL0920-80,ADL0920-135,ADL1020-0K030062 · LIT | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
