Traferox Technologies, Inc. is one of 500 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: X°Port Heart Preservation System, VI°Port™ Liver Preservation System, X°Port Lung Preservation System
4
Total
4
Cleared
0
Denied
Traferox Technologies, Inc. has 4 FDA 510(k) cleared medical devices. Based in Mississauga, CA.
Latest FDA clearance: Sep 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.
4 devices
Cleared
Sep 16, 2026
X°Port Heart Preservation System
Cardiovascular
100d
Cleared
Jun 01, 2026
VI°Port™ Liver Preservation System
Gastroenterology & Urology
110d
Cleared
May 01, 2025
X°Port Lung Preservation System
Gastroenterology & Urology
135d
Cleared
Nov 26, 2024
LungProtect
Gastroenterology & Urology
264d