# SPINECRAFT LLC

FEI: 3004717358
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Owner/operator: SPINECRAFT LLC (#9065601)

Address: 777 Oakmont Ln Suite 200, Westmont, IL, US



## Products

Total registered: 2
Top product codes: MAX, ODP
Regulation §: 888.3080

Proprietary names: ORIO-Ti Intervertebral Body Fusion Cage System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223004717358%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3004717358