FDA Device Establishments · JSON-LD · Markdown

SPINEART SA

FEI 3007728266 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active

FEI Number3007728266
Owner / OperatorSPINEART SA (#10028947)
AddressChemin du Pre-Fleuri 3, Plan-les-Ouates Geneve, 1228, CH
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)MNI, MNH
Regulation § (21 CFR)888.3070
Proprietary namesROMEO

External sources

Source: openFDA. Public-domain (CC0).