Corin, Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Corin, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Raynham, US.
Last cleared in 2021. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Corin, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by BioVera, Inc. as regulatory consultant.
2 devices