Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007038972

FEI Number

3007038972

Entity Name

MAT GMBH & CO. KG

City/State/Country

Emmingen-Liptingen Baden-Wurttemberg, DE

Establishment Address

Friedrich-Woehlerstrasse 10, Emmingen-Liptingen Baden-Wurttemberg 78576, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

MAT GmbH & Co. KG (Owner Number: 10095240)

Owner / Operator Contact Address

Friedrich-Woehlerstrasse 10, Emmingen-Liptingen, DE-BW 78576, DE

Initial Importer Flag

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
HTT	Burr, Orthopedic	Orthopedic	Class 1	888.4540	2026-02-10
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2026-02-10
HTW	Bit, Drill	Orthopedic	Class 1	888.4540	2026-02-10

Official Correspondent

No official correspondent registered.

US Agent Details

Angelika Scherp Business: Business Support International Email: info@bsi-fda.com Phone: (212) 3318358

Related Public Records

Same Entity

MAT GmbH & Co. KG

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0009-2007	Smith & Nephew Inc	1	Journey Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 74018811, 74018813, 74018815, 74018817.
Z-0010-2007	Smith & Nephew Inc	1	Genesis II Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71440480, 71440482, 71440484, 71440486
Z-0011-06	Stryker Howmedica Osteonics Corp.	1	Allocraft TLIF Bone Inserter.
Z-0011-2007	Smith & Nephew Inc	1	Genesis II Oversized Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71927102, 71927103, 71927104, 71927105
Z-0013-2011	Depuy Orthopaedics, Inc.	1	Summit Broach Handle, NON-STERILE, MFG: DEPUY ORTHOPAEDICS, INC., PO BOX 988 WARSAW, IN 46581, 1 800 366 8143 Catalog Number: 2570-00-000 The Summit Broach Handle (instrumentation) is used with the DePuy Summit Tapered Hip System. The Broach Handle is used to prepare the femur for hip system implantation. The broach handle is an impaction/extraction device that holds broaches for creating the cavity in the femur during hip arthroplasty.

Similar Registrations

Registration Number	Establishment Name	Location
3006017180	BBF STERILISATIONSSERVICE GMBH	Kernen Baden-Wurttemberg, DE
2025102	Brasseler U.S.A. Medical, LLC	Savannah, GA, US
3005575604	SURETEK MEDICAL	GREENVILLE, SC, US
3038195984	BEIJING FULE SCIENCE & TECHNOLOGY DEVELOPMENT CO., LTD.	Beijing, CN
3014334038	Integra LifeSciences Production Corporation	Mansfield, MA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007038972. Last updated year: 2026. Please use registration number 3007038972 when referencing this establishment in official correspondence.