FDA Device Establishments · JSON-LD · Markdown

NEONAVIA AB

FEI 3042940295 · Manufacture Medical Device · Status: Active

FEI Number3042940295
Owner / OperatorNeoNavia Ab (#10094565)
AddressStolp-Ekeby 11, Vallentuna Stockholm, 18695, SE
Mandatory US AgentPro Pharma Group
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)KNW, FCG
Regulation § (21 CFR)876.1075
Proprietary namesFlexiPulse, VacuPulse; NeoNavia Biopsy System

External sources

Source: openFDA. Public-domain (CC0).