Creagh Medical Ltd. Dba Surmodics, Inc. is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Creagh Medical Ltd. Dba Surmodics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: 018 Hydrophilic Coated OTW PTA Balloon Dilatation Catheter
1
Total
1
Cleared
0
Denied
Creagh Medical Ltd. Dba Surmodics, Inc. has 1 FDA 510(k) cleared medical devices. Based in Ballinasloe, IE.
Latest FDA clearance: Nov 2024. Active since 2024. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Creagh Medical Ltd. Dba Surmodics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Creagh Medical Ltd. Dba Surmodics, Inc.
1 devices