Anodyne is one of 13028 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Anodyne - FDA 510(k) Cleared Devices
Recent clearances: Oasis Lacrimal Intubation Set
1
Total
0
Cleared
0
Denied
Anodyne has 0 FDA 510(k) cleared medical devices. Based in O' Fallon, US.
Historical record: 0 cleared submissions from 2016 to 2016. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Anodyne Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Anodyne
1 devices