DENTRADE GMBH & CO.KG

FDA Device Registration & Listing · Cologne North Rhine-Westphalia, DE · Registration 3012339007

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
3012339007
FEI Number
3012339007
Entity Name
DENTRADE GMBH & CO.KG
City/State/Country
Cologne North Rhine-Westphalia, DE
Establishment Address
13 Monheimer St., Cologne North Rhine-Westphalia 50737, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Dentrade GmbH & Co.KG (Owner Number: 10088036)
Owner / Operator Contact Address
13 Monheimer St., Cologne, DE-NW 50737, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

RehaSplint

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ELS Splint, Endodontic Stabilizing Dental Class 2 872.3890 2023-05-17

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

Dentrade GmbH & Co.KG
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 3012339007. Last updated year: 2026. Please use registration number 3012339007 when referencing this establishment in official correspondence.
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