FDA applicant
Kestrel
FDA records 3 decisions for Kestrel (Columbus, IN) in 1990: 3 510(k) clearances. All are in product code LRX (Case, Contact Lens). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Kestrel’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Kestrel since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Kestrel’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report