Vein 360, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vein 360, LLC - FDA 510(k) Cleared Devices
Recent clearances: Vein360 Reprocessed Visions PV.014P Rx Digital IVUS Catheter, Vein360 Reprocessed Eagle Eye Platinum Rx Digital IVUS Catheter, Vein360 Reprocessed Eagle Eye Platinum ST Rx Digital IVUS Catheter, Vein360 Reprocessed Visions PV.018 Digital IVUS Catheter, Vein360 Reprocessed Visions PV.035 Digital IVUS Catheter
4
Total
4
Cleared
0
Denied
Vein 360, LLC has 4 FDA 510(k) cleared medical devices. Based in Blue Ash, US.
Last cleared in 2023. Active since 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Vein 360, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vein 360, LLC
4 devices
Cleared
Oct 24, 2023
Vein360 Reprocessed Visions PV.014P Rx Digital IVUS Catheter, Vein360...
Cardiovascular
60d
Cleared
Aug 25, 2023
Vein360 Reprocessed Visions PV.018 Digital IVUS Catheter
Cardiovascular
144d
Cleared
Jun 06, 2023
Vein360 Reprocessed Visions PV.035 Digital IVUS Catheter
Cardiovascular
96d
Cleared
Oct 22, 2019
Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter
General & Plastic Surgery
183d