Episurf Medical, Inc. - FDA 510(k) Cleared Devices
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.
1 devices