FDA Device Establishments · JSON-LD · Markdown

ECHOSENS

FEI 3010258456 · Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active

FEI Number3010258456
Owner / OperatorEchosens (#10043955)
Address6 rue Ferrus, Paris, 75014, FR
Mandatory US AgentEchosens North America
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)ITX, IYO
Regulation § (21 CFR)892.1570, 892.1560
Proprietary namesFibroScan 502 Touch; FibroScan; XL+ probe; M+ probe

External sources

Source: openFDA. Public-domain (CC0).