Edwards Lifesiences, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Edwards Lifesiences, LLC - FDA 510(k) Cleared Devices
Recent clearances: Swang-Ganz IQ pulmonary artery catheter, HemoSphere Advanced Monitoring Platform, HemoSphere ClearSight Module
2
Total
2
Cleared
0
Denied
Edwards Lifesiences, LLC has 2 FDA 510(k) cleared medical devices. Based in Irvine, US.
Last cleared in 2022. Active since 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Edwards Lifesiences, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Edwards Lifesiences, LLC
2 devices