# Intervene

- Location (FDA's records): Redwood City, CA
- FDA decisions: 2 (2023–2025): 2 510(k) clearances
- Names in FDA's records: Intervene (1); Intervene, Inc. (1)
- Product codes: QEW (1), NPG (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
- Inari Medical, Inc.: 1 (https://510kreport.com/company/inari-medical)
- Mercator Medsystems, Inc.: 1 (https://510kreport.com/company/mercator-medsystems)

## Recent decisions
- K251185: Recana Thrombectomy Catheter System (FG014. FG015, FG016, FG017, FG018, FG019, FG020) (Oct 22, 2025)
- K222185: Stratus Infusion Catheter (Apr 13, 2023)

Source page: https://510kreport.com/company/intervene