# VEIN360

FEI: 3015988948
Status: Active
Establishment types: Reprocess Single-Use Device
Owner/operator: Vein360 (#10061626)

Address: 4460 Lake Forest Dr, STE 218, Blue Ash, OH, US



## Products

Total registered: 2
Top product codes: NUJ, GEI
Regulation §: 878.4400


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223015988948%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3015988948