FDA Device Establishments · JSON-LD · Markdown

Aurora Spine Manufacturing

FEI 3020417298 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active

FEI Number3020417298
Owner / OperatorAurora Spine (#10045511)
Address3146 Tiger Run Ct, Suite 116, Carlsbad, CA, US
Registration expiry2026
Initial importer flagN
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).