FDA applicant
Marlin Industries
FDA records 3 decisions for Marlin Industries (Tarzana, CA) in 1985: 3 510(k) clearances. Most are in product codes KYE (Inserter/Remover Contact Lens) and HPX (Lens, Contact (Polymethylmethacrylate)). 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 Marlin Industries’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Marlin Industries since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Marlin Industries’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