FDA applicant
Cuda Products Co.
FDA records 17 decisions for Cuda Products Co. (Jacksonville, FL) from 1988 to 1998: 17 510(k) clearances. Most are in product codes FST (Light, Surgical, Fiberoptic) and FSS (Light, Surgical, Floor Standing). 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 Cuda Products Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Cuda Products Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Cuda Products Co.’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