Dyad Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dyad Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Libby Echo:Prio, Libby IAAA v1.0
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.
FDA 510(k) Regulatory Record - Dyad Medical, Inc.
2 devices