# Avantec Vascular Corp.

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 5 (2003–2026): 5 510(k) clearances
- Names in FDA's records: Avantec Vascular Corp. (3); Avantec Vascular Corporation (2)
- Product codes: FGE (2), MMX (1), QEW (1), LIT (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Merit Medical Systems, Inc.: 2 (https://510kreport.com/company/merit-medical-systems)
- Cook, Inc.: 1 (https://510kreport.com/company/cook)
- Volcano Atheromed, Inc.: 1 (https://510kreport.com/company/volcano-atheromed)

## Firms that cite its devices most
- Onocor Vascular, LLC: 1 (https://510kreport.com/company/onocor-vascular)
- Guidant Corp.: 1 (https://510kreport.com/company/guidant)

## Its most-cited devices
- K170987: Captus Vascular Retrieval System (2017), cited by 1
- K030638: Duramax .035 Biliary Stent System, Models DML0718-80, DML0718-135, DML0818-80, DML0818-135, DML0918-80, DML0918-135, DML (2003), cited by 1

## Recent decisions
- K251207: Sangria™ Thrombectomy System (Jan 7, 2026)
- K170987: Captus Vascular Retrieval System (Aug 28, 2017)
- K032436: Duramax .018 Biliary Stent System (Feb 4, 2004)
- K030638: Duramax .035 Biliary Stent System, Models DML0718-80, DML0718-135, DML0818-80, DML0818-135, DML0918-80, DML0918-135, DML (Jul 9, 2003)
- K030062: Admiral .035 Dilatation Catheter, Models ADL0720-80,ADL0720-135,ADL0820-80, ADL0820-135,ADL0920-80,ADL0920-135,ADL1020-0 (Apr 3, 2003)

Source page: https://510kreport.com/company/avantec-vascular