Artrya Limited is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Artrya Limited - FDA 510(k) Cleared Devices
Recent clearances: Salix Coronary Plaque (V1.0.0), Salix Central
2
Total
2
Cleared
0
Denied
Artrya Limited has 2 FDA 510(k) cleared medical devices. Based in Perth, AU.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Artrya Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Artrya Limited
2 devices