Dyad Medical, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Dyad Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Boston, US.
Last cleared in 2022. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Dyad Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Pharmalex Pty, Ltd. as regulatory consultant.
2 devices