FDA Device Establishments · JSON-LD · Markdown

AMPLIFON

FEI 3002806418 · Manufacture Medical Device · Status: Active

FEI Number3002806418
Owner / OperatorAmplifon (#10060656)
AddressVia Ripamonti 133, Milano, 20141, IT
Mandatory US AgentAmplifon
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)OSM
Regulation § (21 CFR)874.3305
Proprietary namesAmplifon App; Miracle Ear App

External sources

Source: openFDA. Public-domain (CC0).