Dr. Jean Bausch GmbH & Co. KG

FDA Device Registration & Listing · COLOGNE North Rhine-Westphalia, DE · Registration 8010224

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
8010224
FEI Number
3004138471
Entity Name
Dr. Jean Bausch GmbH & Co. KG
City/State/Country
COLOGNE North Rhine-Westphalia, DE
Establishment Address
OSKAR-SCHINDLER STR 4, COLOGNE North Rhine-Westphalia D-50769, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Dr. Jean Bausch GmbH & Co. KG (Owner Number: 8010224)
Owner / Operator Contact Address
Oskar-Schindler-Strasse 4, Cologne, DE-NW D-50769, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

OccluSense ARTICULATING PAPERS Bausch Articulating Paper Forceps Bausch Arti-Fol Forceps

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EFH Paper, Articulation Dental Class 1 872.6140 1989-06-26
EFK Forceps, Articulation Paper Dental Class 1 872.4565 2013-06-27

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Dr. Jean Bausch GmbH & Co. KG
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8010224. Last updated year: 2026. Please use registration number 8010224 when referencing this establishment in official correspondence.
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