# Nuvascular, Inc.

- Location (FDA's records): Irvine, CA
- FDA decisions: 2 (2025–2026): 2 510(k) clearances
- Product codes: KRD (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (1 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
- Aga Medical Corp.: 2 (https://510kreport.com/company/aga-medical)

## Its most-cited devices
- K250133: HARBOR Occlusion Device (2025), cited by 1

## Recent decisions
- K260635: HARBOR Occlusion Device (Jun 12, 2026)
- K250133: HARBOR Occlusion Device (Jul 9, 2025)

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