Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014893827

FEI Number

3014893827

Entity Name

HAAGER GMBH & CO. KG

City/State/Country

Pforzheim Baden-Wurttemberg, DE

Establishment Address

Lochaeckerstrasse 14, Pforzheim Baden-Wurttemberg 75177, DE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Haager GmbH & Co. KG (Owner Number: 10093150)

Owner / Operator Contact Address

Lochaeckerstrasse 14, Pforzheim, DE-BW 75177, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Insertion Aid

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FGB	Ureteroscope And Accessories, Flexible/Rigid	Gastroenterology, Urology	Class 2	876.1500	2025-04-07

Official Correspondent

Clemens Winkler

US Agent Details

Anja Fair Business: Karl Storz Email: anja.fair@karlstorz.com Phone: (424) 2188247

Related Public Records

Same Entity

Haager 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
K915458	Psi Medical Products, Inc.	URETEROSCOPE	1992-01-30

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014893827. Last updated year: 2026. Please use registration number 3014893827 when referencing this establishment in official correspondence.