Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009936738

FEI Number

3009936738

Entity Name

Condor MedTec GmbH

City/State/Country

Salzkotten North Rhine-Westphalia, DE

Establishment Address

Dr.-Krismann-Str. 15, Salzkotten North Rhine-Westphalia 33154, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Condor MedTec GmbH (Owner Number: 10047183)

Owner / Operator Contact Address

Dr.-Krismann-Str. 15, Salzkotten, DE-NW 33154, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

RotexTable by Condor® RotexShoe by Condor®

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KQZ	Component, Traction, Non-Invasive	Orthopedic	Class 1	888.5890	2014-07-14

Official Correspondent

Heidi Brautmeier

US Agent Details

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

Related Public Records

Same Entity

Condor MedTec GmbH

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009936738. Last updated year: 2026. Please use registration number 3009936738 when referencing this establishment in official correspondence.