Technopath Manufacturing is one of 45 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Technopath Manufacturing - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Technopath Manufacturing has 1 FDA 510(k) cleared medical devices. Based in Ballina, IE.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Technopath Manufacturing Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Technopath Manufacturing
1 devices