Idx, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Idx, LLC - FDA 510(k) Cleared Devices
1
Total
0
Cleared
1
Denied
Idx, LLC has 0 FDA 510(k) cleared medical devices. Based in Iowa City, US.
Active since 2018. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Idx, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Idx, LLC
1 devices