S.U.A. MARTIN GMBH & CO.

FDA Device Registration & Listing · RIETHEIM-WEILHEIM Baden-Wurttemberg, DE · Registration 8010386

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
8010386
FEI Number
3000178338
Entity Name
S.U.A. MARTIN GMBH & CO.
City/State/Country
RIETHEIM-WEILHEIM Baden-Wurttemberg, DE
Establishment Address
UHLANDSTR. 17, RIETHEIM-WEILHEIM Baden-Wurttemberg 78604, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
S.U.A. MARTIN GMBH & CO.KG (Owner Number: 8010386)
Owner / Operator Contact Address
UHLANDSTR. 17, --, RIETHEIM-WEILHEIM, DE-NOTA 78604, 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
HAE Rongeur, Manual Neurology Class 2 882.4840 2007-11-23
LRW Scissors, General, Surgical General, Plastic Surgery Class 1 878.4800 2013-01-23
LXH Orthopedic Manual Surgical Instrument Orthopedic Class 1 888.4540 2012-05-24
GZX Instrument, Microsurgical Neurology Class 1 882.4525 1998-11-10
HTD Forceps General, Plastic Surgery Class 1 878.4800 2010-03-17
KBD Scissors, Nasal Ear, Nose, Throat Class 1 874.4420 2002-07-17
FHQ Holder, Needle, Gastroenterologic Gastroenterology, Urology Class 1 876.4730 1998-11-10
FSM Tray, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 2013-05-21
HAE Rongeur, Manual Neurology Class 2 882.4840 2015-09-18
HXK Holder, Needle; Orthopedic Orthopedic Class 1 888.4540 2013-01-23
HTX Rongeur Orthopedic Class 1 888.4540 1998-12-04

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

S.U.A. MARTIN 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
K852723 The Huxley Instrument Corp. FOERSTER SPONGE FORCEPS, SERRATED, 7+SS 410 OR 420 1985-07-15
K873512 Arthropedics, Inc. SERRATED GRASPING FORCEPS, RIGHT 1987-11-02

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
8010769 KAPP SURGICAL GMBH DUERBHEIM Baden-Wurttemberg, DE
9680515 TONTARRA MEDIZINTECHNIK GMBH WURMLINGEN Baden-Wurttemberg, DE
9710524 ULTIMATE MEDICAL PRODUCTS LTD. SHARJAH Ash Shariqah, AE
1836161 ASPEN SURGICAL PRODUCTS, INC. Caledonia, MI, US
8010697 GEISTER MEDIZINTECHNIK GMBH TUTTLINGEN Baden-Wurttemberg, DE
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8010386. Last updated year: 2026. Please use registration number 8010386 when referencing this establishment in official correspondence.
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