AbbVie is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
AbbVie - FDA 510(k) Cleared Devices
Recent clearances: Natrelle 133S Tissue Expanders
1
Total
1
Cleared
0
Denied
AbbVie has 1 FDA 510(k) cleared medical devices. Based in Irvine, US.
Latest FDA clearance: Jan 2026. Active since 2026. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by AbbVie Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - AbbVie
1 devices