# Jupiter Endovascular

- Location (FDA's records): Menlo Park, CA
- FDA decisions: 2 (2025–2026): 2 510(k) clearances
- Product codes: DYB (1), QEW (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (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
- W. L. Gore & Associates, Inc.: 1 (https://510kreport.com/company/w-l-gore-associates)
- Imperative Care, Inc.: 1 (https://510kreport.com/company/imperative-care)

## Recent decisions
- K261523: Vertex™ Thrombectomy System (Aug 4, 2026)
- K252027: Vertex (TM) Catheter (Sep 12, 2025)

Source page: https://510kreport.com/company/jupiter-endovascular