Veinrx, Inc. is one of 22293 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Veinrx, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VARICATH PERIPHERAL INFUSION CATHETER, INFUSIONCATH PERIPHERAL INFUSION CATHETER, MODELS VF0012, VF0016, VF0024, VF0028, VF0032, VF0036, VF0040, VF0044
2
Total
2
Cleared
0
Denied
Veinrx, Inc. has 2 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 2 cleared submissions from 2005 to 2007. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Veinrx, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Veinrx, Inc.
2 devices