FDA applicant
Ati
FDA records 3 decisions for Ati (Los Angeles, CA) from 1989 to 1990: 3 510(k) clearances. Most are in product codes ILO (Pack, Hot Or Cold, Water Circulating) and FRC (Indicator, Biological Sterilization Process). 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 Ati’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Ati since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Ati’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