Abbott Ireland is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Abbott Ireland has 2 FDA 510(k) cleared medical devices. Based in Lisnamuck, IE.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Abbott Ireland Filter by specialty or product code using the sidebar.
1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
FDA 510(k) Regulatory Record - Abbott Ireland
2 devices