# Aura Lens Products

- Location (FDA's records): St. Cloud, MN
- FDA decisions: 2 (1985–1987): 2 510(k) clearances
- Product codes: HQG (2)
- 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
- K872506: Melanite I (Jul 27, 1987)
- K852403: Auralite II (Aug 20, 1985)

Source page: https://510kreport.com/company/aura-lens-products