Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015462848

FEI Number

3015462848

Entity Name

OSSENBRUEGGEN FEINWERKTECHNIK GMBH & CO. KG

City/State/Country

Moorrege Schleswig-Holstein, DE

Establishment Address

Wedeler Chaussee 56d, Moorrege Schleswig-Holstein 25436, DE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Ossenbrueggen Feinwerktechnik GmbH & Co. KG (Owner Number: 10060347)

Owner / Operator Contact Address

Wedeler Chaussee 56d, Moorrege, DE-SH 25436, DE

Initial Importer Flag

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
PGW	Ear, Nose, And Throat Stereotaxic Instrument	Neurology	Class 2	882.4560	2019-04-29

Official Correspondent

Stefan Hueners

US Agent Details

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

Related Public Records

Same Entity

Ossenbrueggen Feinwerktechnik 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
K200041	Fiagon GmbH	FlexPointer 1.5 Single Use, FlexTube 3 Single Use	2020-03-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015462848. Last updated year: 2026. Please use registration number 3015462848 when referencing this establishment in official correspondence.