SCHELLENBERGER BUERSTENFABRIK GMBH

FDA Device Registration & Listing · Bechhofen Bavaria, DE · Registration 3009935038

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
3009935038
FEI Number
3009935038
Entity Name
SCHELLENBERGER BUERSTENFABRIK GMBH
City/State/Country
Bechhofen Bavaria, DE
Establishment Address
Rudolf-Diesel-Strasse 17, Bechhofen Bavaria 91572, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Schellenberger Buerstenfabrik GmbH (Owner Number: 10044123)
Owner / Operator Contact Address
Rudolf-Diesel-Strasse 17, Bechhofen, DE-BY 91572, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Curaprox Interdental Brush

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EFW Toothbrush, Manual Dental Class 1 872.6855 2013-05-02

Official Correspondent

Gisela Schellenberger

US Agent Details

German American Chamber of Commerce, Inc. German American Ch Email: legalservices@gaccny.com Phone: (212) 9748830

Related Public Records

Same Entity

Schellenberger Buerstenfabrik GmbH
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
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009935038. Last updated year: 2026. Please use registration number 3009935038 when referencing this establishment in official correspondence.
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