SPIEGELBERG GmbH & Co. KG

FDA Device Registration & Listing · Hamburg, DE · Registration 3002108226

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
3002108226
FEI Number
3002108226
Entity Name
SPIEGELBERG GmbH & Co. KG
City/State/Country
Hamburg, DE
Establishment Address
Tempowerkring 4, Hamburg 21079, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Spiegelberg GmbH & Co. KG (Owner Number: 10037562)
Owner / Operator Contact Address
Tempowerkring 4, Hamburg, DE-HH 21079, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
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
GZX Instrument, Microsurgical Neurology Class 1 882.4525 2013-06-04
GWM Device, Monitoring, Intracranial Pressure Neurology Class 2 882.1620 2011-07-26

Official Correspondent

Stefan Paschko

US Agent Details

Stephen Lieberman Business: Donawa Lifescience, Inc Email: lieberman@donawa.com Phone: (561) 3020777

Related Public Records

Same Entity

Spiegelberg 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
K020558 Integra Neurosciences LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE 2002-03-21

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3002108226. Last updated year: 2026. Please use registration number 3002108226 when referencing this establishment in official correspondence.
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