FDA Device Establishments · JSON-LD · Markdown

AURORA SPINE, INC.

FEI 3010326971 · Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active

FEI Number3010326971
Owner / OperatorAurora Spine (#10045511)
Address1930 Palomar Point Way, Suite #103, Carlsbad, CA, US
Registration expiry2026
Initial importer flagY
Registered products1
Product codes (top 20)PEK
Regulation § (21 CFR)888.3050
Proprietary namesZIP MIS Interspinous Fusion System; ZIP ULTRA MIS Interspinous Fusion System; SILO TFX

External sources

Source: openFDA. Public-domain (CC0).