Episurf Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Episurf Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Episealer Patellofemoral System
1
Total
1
Cleared
0
Denied
Episurf Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Last cleared in 2022. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Episurf Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Episurf Medical, Inc.
1 devices