Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

8010235

FEI Number

3004369356

Entity Name

SIEMA-SIEGFRIED MARTIN GMBH

City/State/Country

WURMLINGEN Baden-Wurttemberg, DE

Establishment Address

WEILHEIMERSTRASSE 20, WURMLINGEN Baden-Wurttemberg 78573, DE

Establishment Type(s)

Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

SIEMA-SIEGFRIED MARTIN GMBH (Owner Number: 8010235)

Owner / Operator Contact Address

WEILHEIMERSTR. 20, --, WURMLINGEN, BW, DE-BW D-78573, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MDS0728219 MDS0728418 MDS0724865

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2020-12-22
DWS	Instruments, Surgical, Cardiovascular	Cardiovascular	Class 1	870.4500	2008-11-17
NNU	Scissors, Wire Cutting, Ent, Non-Sterile	Ear, Nose, Throat	Class 1	874.3540	2008-11-17
EGN	Scissors, Surgical Tissue, Dental	Dental	Class 1	872.4565	1984-02-10
HXZ	Cutter, Wire	Orthopedic	Class 1	888.4540	1999-11-03
JZB	Scissors, Ear	Ear, Nose, Throat	Class 1	874.4420	1999-11-03
HRR	Scissors, Orthopedic, Surgical	Orthopedic	Class 1	888.4540	1995-11-29
KBD	Scissors, Nasal	Ear, Nose, Throat	Class 1	874.4420	1999-11-03
LRW	Scissors, General, Surgical	General, Plastic Surgery	Class 1	878.4800	1999-11-03
HDJ	Scissors, Umbilical	Obstetrics/Gynecology	Class 1	884.4520	1999-11-03
HNF	Scissors, Ophthalmic	Ophthalmic	Class 1	886.4350	1999-11-03

Official Correspondent

No official correspondent registered.

US Agent Details

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

Related Public Records

Same Entity

SIEMA-SIEGFRIED MARTIN GMBH

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
K821275	Conphar, Inc.	MAYO SCISSOR STRAIGHT 5 1/2	1982-05-28
K914226	E.I. Dupont DE Nemours & Co., Inc.	ACA(R) BETA-2-MICROGLOBULIN (B2M) TEST PACK	1991-11-19

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.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8010235. Last updated year: 2026. Please use registration number 8010235 when referencing this establishment in official correspondence.