# Aurex SA (Pty), Ltd.

- Location (FDA's records): Edenvale, Gauteng, ZA
- FDA decisions: 6 (2000–2000): 6 510(k) clearances
- Product codes: EJT (6)
- Predicates its devices cite: 0 (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

## Recent decisions
- K001481: Palceram 49 (Jun 23, 2000)
- K001482: Aurenorm 75 KF (Jun 23, 2000)
- K001480: Aurecast 40 B (Jun 21, 2000)
- K001479: Palceram 53 (Jun 21, 2000)
- K001478: Aurecast Super Inlay (Jun 20, 2000)
- K001477: Aurelux Y 84 Premium (Jun 20, 2000)

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