Puracath Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Puracath Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PuraCath Firefly Needleless Connector IT (9005), Firefly Needleless Connector
3
Total
3
Cleared
0
Denied
Puracath Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Newark, US.
Latest FDA clearance: Feb 2026. Active since 2016. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Puracath Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Puracath Medical, Inc.
3 devices