# Innovize

FEI: 3007867940
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: Innovize (#10026450)

Address: 500 Oak Grove Parkway, North Oaks, MN, US



## Products

Total registered: 1
Top product codes: FZZ
Regulation §: 878.4660


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223007867940%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3007867940