AURELIYM GMBH

FDA Device Registration & Listing · Bad Neuenahr-Ahrweiler Rhineland-Palatinate, DE · Registration 3026390997

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
3026390997
FEI Number
3026390997
Entity Name
AURELIYM GMBH
City/State/Country
Bad Neuenahr-Ahrweiler Rhineland-Palatinate, DE
Establishment Address
Hauptstrasse 96, Bad Neuenahr-Ahrweiler Rhineland-Palatinate 53474, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Aureliym GmbH (Owner Number: 10087268)
Owner / Operator Contact Address
Hauptstrasse 96, Bad Neuenahr-Ahrweiler, DE-RP 53474, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K221125
PMA Number
N/A

All Registered Proprietary Names

SilentCloud

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KLW Masker, Tinnitus Ear, Nose, Throat Class 2 874.3400 2023-02-14

Official Correspondent

Alexander Wegener

US Agent Details

Becky Lucas Business: Connect Hearing USA Email: becky.lucas@sonova.com Phone: (331) 7020225

Related Public Records

Same Entity

Aureliym GmbH
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 3026390997. Last updated year: 2026. Please use registration number 3026390997 when referencing this establishment in official correspondence.
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