Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

8010839

FEI Number

6507

Entity Name

MM MEDER

City/State/Country

TUTTLINGEN Baden-Wurttemberg, DE

Establishment Address

ETTLENSEGART 40, TUTTLINGEN Baden-Wurttemberg 78532, DE

Establishment Type(s)

Repack or Relabel Medical Device,Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

MM MEDER (Owner Number: 8010839)

Owner / Operator Contact Address

ETTLENSEGART 40, --, TUTTLINGEN, DE-BW 78532, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Marlene Meder Marlene Meder

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HXZ	Cutter, Wire	Orthopedic	Class 1	888.4540	2010-04-02
DZN	Instruments, Dental Hand	Dental	Class 1	872.4565	2010-04-02

Official Correspondent

Erich MEDER

US Agent Details

Daniel Meder Business: Meder Distributing, Inc. Email: dan@mm-meder.com Phone: (219) 7973610

Related Public Records

Same Entity

MM MEDER

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3012995405	SURGIX MEDICAL LLC	Spring, TX, US
3002862271	Wenzler Medizintechnik GmbH	Frittlingen Baden-Wurttemberg, DE
8010733	PRO-MED INSTRUMENTE GMBH	TUTTLINGEN Baden-Wurttemberg, DE
3015895045	Sklar Corporation - Warehouse	Salisbury, MD, US
2132732	TECOMET, INC.	KENOSHA, WI, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8010839. Last updated year: 2026. Please use registration number 8010839 when referencing this establishment in official correspondence.