MedXpert GmbH

FDA Device Registration & Listing · Eschbach Baden-Wurttemberg, DE · Registration 3006801247

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
3006801247
FEI Number
3006801247
Entity Name
MedXpert GmbH
City/State/Country
Eschbach Baden-Wurttemberg, DE
Establishment Address
Max-Immelmann-Allee 19, Eschbach Baden-Wurttemberg 79427, DE
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
MedXpert GmbH (Owner Number: 10023342)
Owner / Operator Contact Address
Max-Immelmann-Allee 19, Eschbach, DE-BW 78427, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K073556
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
MDM Instrument, Manual, Surgical, General Use General, Plastic Surgery Class 1 878.4800 2007-11-19
HRS Plate, Fixation, Bone Orthopedic Class 2 888.3030 2008-06-25

Official Correspondent

Johannes Mussler

US Agent Details

Franz Menean Business: MEDAGENT Inc. Email: mail@medagent-usa.com Phone: (603) 5702039

Related Public Records

Same Entity

MedXpert 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
K042598 Zimmer, Inc. PERIARTICULAR LOCKING PLATES AND SCREWS, 2357 AND 2359 SERIES 2004-10-29
K190842 Jiangsu Trauhui Medical Instrument Co., Ltd. Comus Locking Plate systems 2020-02-03
K130510 Arthrex, Inc. ARTHREX COMPRESSION PLATES 2013-09-25
K202803 Newclip Technics Activmotion S DTO 2021-12-16

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0034-2022 Flower Orthopedics Corporation 2
Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006801247. Last updated year: 2026. Please use registration number 3006801247 when referencing this establishment in official correspondence.
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