Drendel + Zweiling DIAMANT GmbH

FDA Device Registration & Listing · Kalletal North Rhine-Westphalia, DE · Registration 9611505

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
9611505
FEI Number
3002806852
Entity Name
Drendel + Zweiling DIAMANT GmbH
City/State/Country
Kalletal North Rhine-Westphalia, DE
Establishment Address
Schuerenbreder Weg 27, Kalletal North Rhine-Westphalia D-32689, DE
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Repack or Relabel Medical Device
Owner / Operator
DRENDEL & ZWEILING DIAMANT GMBH (Owner Number: 8010579)
Owner / Operator Contact Address
27, SCHUERENBREDER WEG, KALLETAL, DE-NOTA 32689, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DENTAL DIAMONDS ECOLINE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DZP Instrument, Diamond, Dental Dental Class 1 872.4535 1981-02-15

Official Correspondent

Sandra Rabe

US Agent Details

Imke Lindenbeck Business: Komet USA LLC Email: ilindenbeck@kometusa.com Phone: (803) 3231504

Related Public Records

Same Entity

DRENDEL & ZWEILING DIAMANT GMBH
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9611505. Last updated year: 2026. Please use registration number 9611505 when referencing this establishment in official correspondence.
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