Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3001065024

FEI Number

3001065024

Entity Name

RENFERT GMBH

City/State/Country

HILZINGEN Baden-Wurttemberg, DE

Establishment Address

UNTERE GIESSWIESEN 2, HILZINGEN Baden-Wurttemberg 78247, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

RENFERT GMBH (Owner Number: 9052056)

Owner / Operator Contact Address

Untere Giesswiesen 2, --, Hilzingen, DE-BW 78247, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SYMPRESS DUOMIX DUOMIX II PROMIX one SYMPRESS II Dynamix Speed 2 temp:ex help:ex discolor f help:ex plaque p help:ex plaque f

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EFD	Amalgamator, Dental, Ac-Powered	Dental	Class 1	872.3100	2007-07-16
NUX	Cleanser, Denture, Prescription	Dental	Class 1	872.3520	2017-11-13

Official Correspondent

Maik Witt

US Agent Details

Janelle Herr Business: RENFERT USA INC. Email: janelle.herr@renfertusa.com Phone: (630) 5497377

Related Public Records

Same Entity

RENFERT 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 3001065024. Last updated year: 2026. Please use registration number 3001065024 when referencing this establishment in official correspondence.