Intricon Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intricon Corporation - FDA 510(k) Cleared Devices
Recent clearances: Lumen 155-SF
1
Total
1
Cleared
0
Denied
Intricon Corporation has 1 FDA 510(k) cleared medical devices. Based in Arden Hills, US.
Last cleared in 2023. Active since 2023. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Intricon Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Intricon Corporation
1 devices