# AURORA SPINE, INC.

FEI: 3010326971
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
Owner/operator: Aurora Spine (#10045511)

Address: 1930 Palomar Point Way, Suite #103, Carlsbad, CA, US



## Products

Total registered: 1
Top product codes: PEK
Regulation §: 888.3050

Proprietary names: ZIP MIS Interspinous Fusion System, ZIP ULTRA MIS Interspinous Fusion System, SILO TFX

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223010326971%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3010326971