Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Vein 360, LLC

US

Last updated May 23, 2026

Information

Country
US
Address
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
—

Catalogue (22)

DeviceModel / ReferenceRegistriesClassStatus
Reprocessed Visions PV.018 Digital IVUS Catheter VEN-PV-018
FDA UDI
Class IIActive
Endovenous Radiofrequency Ablation (RFA) Catheter VEN-7-100
FDA UDI
Class IIUnknown
Vein360 Reprocessed Visions PV.014P RX Digitial IVUS Catheter (014P) VEN-PV-014P
FDA UDI
Class IIActive
Vein360 Reprocessed Visions PV.014P RX Digitial IVUS Catheter (014P) 85910PRH
FDA UDI
Class IIActive
Endovenous Radiofrequency Ablation (RFA) Catheter VEN-7-100
FDA UDI
Class IIActive
Vein360 Reprocessed Eagle Eye Platinum Rx Digital IVUS Catheter VEN-PV-EEP
FDA UDI
Class IIActive
Reprocessed Visions PV.035 Digital IVUS Catheter VEN-PV-035
FDA UDI
Class IIActive
Vein360 Reprocessed Visions PV.014P RX Digital IVUS Catheter (014R) 014RRH
FDA UDI
Class IIActive
Vein360 Reprocessed Eagle Eye Platinum Rx Digital IVUS Catheter 85900PRH
FDA UDI
Class IIActive
Vein360 Reprocessed Visions PV.035 Digital IVUS Catheter 88901RH
FDA UDI
Class IIActive
Endovenous Radiofrequency Ablation (RFA) Catheter VEN-7-60
FDA UDI
Class IIUnknown
Vein360 Reprocessed Eagle Eye Platinum ST Rx Digital IVUS Catheter 85900PSTRH
FDA UDI
Class IIActive
Endovenous Radiofrequency Ablation (RFA) Catheter VEN-3-60
FDA UDI
Class IIUnknown
Endovenous Radiofrequency Ablation (RFA) Catheter VEN-7-60
FDA UDI
Class IIActive
Vein360 Reprocessed Eagle Eye Platinum ST Rx Digital IVUS Catheter VEN-PV-EEPST
FDA UDI
Class IIActive
Endovenous Radiofrequency Ablation (RFA) Catheter VEN-3-60
FDA UDI
Class IIActive
Vein360 Reprocessed Digital Intravascular (IVUS) Reprocessed Catheter PV .018 86700RH
FDA UDI
Class IIActive
Vein360 Reprocessed Visions PV.014P RX Digital IVUS Catheter (014R) VEN-PV-014R
FDA UDI
Class IIActive
Vein360 Reprocessed Visions PV.018 Digital IVUS Catheter K230928
FDA 510(k)
Class IIActive
Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter K191073
FDA 510(k)
Class IIActive
Vein360 Reprocessed Visions PV.035 Digital IVUS Catheter K230584
FDA 510(k)
Class IIActive
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 K232584
FDA 510(k)
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.