# Embolization Inc

FEI: 3042953152
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Boulder iQ (#10094690)

Address: 5421 Western Ave, Boulder, CO, US



## Products

Total registered: 1
Top product codes: KRD
Regulation §: 870.3300

Proprietary names: Nitinol Enhanced Device (NED)

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223042953152%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3042953152