Avery Dennison Medical , Ltd. is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Avery Dennison Medical , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: BeneHold™ Surgical Incise Drape with CHG antimicrobial II
1
Total
1
Cleared
0
Denied
Avery Dennison Medical , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Longford, IE.
Last cleared in 2023. Active since 2023. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Avery Dennison Medical , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Avery Dennison Medical , Ltd.
1 devices