FREUDENBERG MEDICAL EUROPE GMBH

FDA Device Registration & Listing · Kaiserslautern Rhineland-Palatinate, DE · Registration 3013445086

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
3013445086
FEI Number
3013445086
Entity Name
FREUDENBERG MEDICAL EUROPE GMBH
City/State/Country
Kaiserslautern Rhineland-Palatinate, DE
Establishment Address
Liebigstrasse 2-8, Kaiserslautern Rhineland-Palatinate 67661, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Freudenberg Medical Europe GmbH (Owner Number: 10093787)
Owner / Operator Contact Address
Liebigstrasse 2-8, Kaiserslautern, DE-RP 67661, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

eXciteOSA

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QNO Neuromuscular Tongue Muscle Stimulator For The Reduction Of Snoring And Obstructive Sleep Apnea Dental Class 2 872.5575 2025-07-10

Official Correspondent

Van Nguyen

US Agent Details

Rhonda Kops Business: Freudenberg Medical LLC Email: regulatoryaffairs@freudenbergmedical.com Phone: (262) 8040860

Related Public Records

Same Entity

Freudenberg Medical Europe 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 3013445086. Last updated year: 2026. Please use registration number 3013445086 when referencing this establishment in official correspondence.
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