FDA.reportPublic FDA data

VEIN360

Matched from indexed company URL: Vein360 LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30159889483015988948VEIN3601N2026-01-014460 Lake Forest Dr STE 218 Blue Ash OH US 45242

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2348511791367686K232584Vein360 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 CatheterOWQ2023-10-24
2348511237856311K230928Vein360 Reprocessed Visions PV.018 Digital IVUS CatheterOWQ2023-08-25
2348511854661550K230584Vein360 Reprocessed Visions PV.035 Digital IVUS CatheterOWQ2023-06-06
2348511302463330K191073Vein360 Endovenous Radiofrequency Ablation (RFA) CatheterNUJ2019-10-22

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
OWQ32023-10-24
NUJ12019-10-22

PMN#

GUDID#