# Core-Nexus

- Location (FDA's records): Encino, CA
- FDA decisions: 2 (2013–2013): 2 510(k) clearances
- Product codes: KWQ (1), MNI (1)
- Predicates its devices cite: 4 (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
- Dio Medical Co., Ltd.: 4 (https://510kreport.com/company/dio-medical)

## Recent decisions
- K131522: Core Pedicle Screw System (Aug 9, 2013)
- K131520: Nexus Anterior Cervical Plate System (Jul 11, 2013)

Source page: https://510kreport.com/company/core-nexus