FDA Device Establishments · JSON-LD · Markdown

NOVOSOURCE, LLC

FEI 3014273644 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active

FEI Number3014273644
Owner / OperatorNovoSource LLC (#10056859)
Address1000 HAMPTON CTR STE A, Morgantown, WV, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)JWH
Regulation § (21 CFR)888.3560
Proprietary namesNovoSource Knee System

External sources

Source: openFDA. Public-domain (CC0).