medi-G GMBH

FDA Device Registration & Listing · Messkirch Baden-Wurttemberg, DE · Registration 3001614464

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
3001614464
FEI Number
3001614464
Entity Name
medi-G GMBH
City/State/Country
Messkirch Baden-Wurttemberg, DE
Establishment Address
Industriepark 1, Messkirch Baden-Wurttemberg 88605, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
medi-G GmbH (Owner Number: 10058204)
Owner / Operator Contact Address
Industriepark 1, Meßkirch, DE-BW 88605, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Metallhandgriffe Nadelhalter Orthopedic manual surgical instrument Nadelhalter Hochdruck-Handgriff Metall-Handgriff ohne Raste Universalgriff, 2 Griffringe Dreiringgriff

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MDM Instrument, Manual, Surgical, General Use General, Plastic Surgery Class 1 878.4800 2018-07-27
GCJ Laparoscope, General & Plastic Surgery Gastroenterology, Urology Class 2 876.1500 2018-07-27
LXH Orthopedic Manual Surgical Instrument Orthopedic Class 1 888.4540 2018-07-27
GCJ Laparoscope, General & Plastic Surgery Gastroenterology, Urology Class 2 876.1500 2018-07-27
EOB Nasopharyngoscope (Flexible Or Rigid) Ear, Nose, Throat Class 2 874.4760 2018-07-27
LRC Instrument, Ent Manual Surgical Ear, Nose, Throat Class 1 874.4420 2018-07-27
CCW Laryngoscope, Rigid Anesthesiology Class 1 868.5540 2018-07-27
FBO Cystourethroscope Gastroenterology, Urology Class 2 876.1500 2018-07-27

Official Correspondent

Oliver Ueth

US Agent Details

Anja Fair Business: Karl Storz Email: Anja.Fair@karlstorz.com Phone: (424) 2188738

Related Public Records

Same Entity

medi-G 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
K914997 Conmedcorp ASP-IRRATOR 1992-01-07
K153773 Olympus Medical Systems Corp. Disposal Lens Cleaning Sheath 2016-11-22
K940141 Micro-Medical Devices, Inc. LAPARAOSCOPES ELECTRONIC WITH STERILE SHEATH 1994-05-19
K933812 Advanced Surgical, Inc. ADVANCED SURGICAL, INC. CANNULA CLEANING DEVICE AND ACCESSORIES 1993-12-13
K254228 Karl Storz SE & CO. KG KARL STORZ Trocars with Valve Seals 2026-05-11

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0027-2009 Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa 2
Applied Medical, Lap Banding Kit, REF: K0398 Contains: (2) C0Q04, 5x100mm Threaded Kii Access System (1) C0604, 15x100mm Non-Threaded Separator System w/Universal Seal, for laparoscopic procedures.
Z-0028-2009 Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa 2
Applied Medical, Lap Banding Kit, REF: K0406 Contains: (1) C0658, 11x100mm Threaded Shielded Trocar w/Universal Seal (1) C0522, 5x100mm Threaded Premium Flat Blade (1) C2202, 150mm Insufflation needle (1) C0605, 15x100mm Threaded Separator Access System (1) CB030, 5mm x 35cm Direct Drive Disposable Scissors (2) C4120, 5mm x 38cm Direct Drive Grasper Reposable Cartridge, for laparoscopic procedures.
Z-0029-2009 Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa 2
Applied Medical, Lap Roux-EN-Y Kit, REF: K2129 Contains: (1) C0Q04, 5x100mm Threaded Kii Access System (1) C0130, 12x100mm Optical Separator System, Non-handled (2) C0Q10, 5x100mm Threaded Kii Cannula and Seal (1) C0605, 15mmx100mm Threaded Cannula System, for laparoscopic procedures.
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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3001614464. Last updated year: 2026. Please use registration number 3001614464 when referencing this establishment in official correspondence.
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