Terragene is one of 7 FDA 510(k) medical device manufacturers from Argentina in the dataset, ranked by real submission volume.
Terragene - FDA 510(k) Cleared Devices
Recent clearances: Terragene® Bionova® BT20 Biological Indicator
1
Total
1
Cleared
0
Denied
Terragene has 1 FDA 510(k) cleared medical devices. Based in Alvear, AR.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Terragene Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Terragene
1 devices