# Kestrel

- Location (FDA's records): Columbus, IN
- FDA decisions: 3 (1990–1990): 3 510(k) clearances
- Product codes: LRX (3)
- 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
- K901748: Kestrel Lens Case (208-12NT Polystyrene) (May 31, 1990)
- K900053: Kestrel Lens Case 731H-893S/P-1700-2611 (Jan 30, 1990)
- K900054: Kestrel Lens Case 1543-893S/P-1700-2611 (Jan 30, 1990)

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