DR. WITTMANN GMBH & CO. KG

FDA Device Registration & Listing · Zwingenberg Hesse, DE · Registration 3006611932

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
3006611932
FEI Number
3006611932
Entity Name
DR. WITTMANN GMBH & CO. KG
City/State/Country
Zwingenberg Hesse, DE
Establishment Address
Rieslingstr. 8, Zwingenberg Hesse 64673, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Dr. Wittmann GmbH & Co. KG (Owner Number: 10090864)
Owner / Operator Contact Address
Rieslingstr. 8, Zwingenberg, DE-HE 64673, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EJR Agent, Polishing, Abrasive, Oral Cavity Dental Class 1 872.6030 2025-02-13

Official Correspondent

No official correspondent registered.

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@ul.com Phone: (512) 3279997

Related Public Records

Same Entity

Dr. Wittmann GmbH & Co. KG
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K121698 Dentsply International, Inc. NUPRO SENSODYNE PROPHYLAXIS PASTE WITH NOVAMIN 2012-08-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006611932. Last updated year: 2026. Please use registration number 3006611932 when referencing this establishment in official correspondence.
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