AMPLIFON

FDA Device Registration & Listing · Milano, IT · Registration 9611864

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
9611864
FEI Number
3002806418
Entity Name
AMPLIFON
City/State/Country
Milano, IT
Establishment Address
Via Ripamonti 133, Milano 20141, IT
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Amplifon (Owner Number: 10060656)
Owner / Operator Contact Address
Via Ripamonti 133, Milano, IT-MI 20141, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Amplifon App; Miracle Ear App

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OSM Hearing Aid, Air-Conduction With Wireless Technology, Prescription Ear, Nose, Throat Class 2 874.3305 2019-06-07

Official Correspondent

No official correspondent registered.

US Agent Details

Shruti Kulkarni Business: Amplifon Email: shruti.kulkarni@amplifon.com Phone: (413) 3740019

Related Public Records

Same Entity

Amplifon
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9611864. Last updated year: 2026. Please use registration number 9611864 when referencing this establishment in official correspondence.
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