Traferox Technologies, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Traferox Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VI°Port™ Liver Preservation System, X°Port Lung Preservation System, LungProtect
3
Total
3
Cleared
0
Denied
Traferox Technologies, Inc. has 3 FDA 510(k) cleared medical devices. Based in Mississauga, CA.
Latest FDA clearance: Jun 2026. Active since 2024. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Traferox Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Traferox Technologies, Inc.
3 devices