FDA applicant
Kaylight Corporation
FDA records 1 decision for Kaylight Corporation (Woodbury, CT) in 2004: 1 510(k) clearance. All are in product code ILY (Lamp, Infrared, Therapeutic Heating). 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 Kaylight Corporation’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Kaylight Corporation since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Kaylight Corporation’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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