E. HAHNENKRATT GMBH

FDA Device Registration & Listing · KOENIGSBACH-STEIN Baden-Wurttemberg, DE · Registration 8010445

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
8010445
FEI Number
4395
Entity Name
E. HAHNENKRATT GMBH
City/State/Country
KOENIGSBACH-STEIN Baden-Wurttemberg, DE
Establishment Address
BENZSTR. 19, KOENIGSBACH-STEIN Baden-Wurttemberg D75203, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
E. HAHNENKRATT GMBH (Owner Number: 8010445)
Owner / Operator Contact Address
BENZSTR. 19, --, KOENIGSBACH-STEIN, DE-NOTA DE75203, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

HAHNENKRATT-MATRIX-BANDS HAHNENKRATT DRILLS HAHNENKRATT-JACKET-CROWN-POST HAHNENKRATT-ROOT-PINS HAHNENKRATT-HANDLES HAHNENKRATT-COPPER BANDS HAHNENKRATT-LARYNGEAL MIRRORS HAHNENKRATT-MATRIX-RETAINER

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DZN Instruments, Dental Hand Dental Class 1 872.4565 1979-07-12
DZA Drill, Dental, Intraoral Dental Class 1 872.4130 2002-07-16
ELR Post, Root Canal Dental Class 1 872.3810 1979-07-12
EJB Handle, Instrument, Dental Dental Class 1 872.4565 1979-07-12
KCQ Tube Impression And Matrix Dental Class 1 872.6570 1979-07-12
KAI Mirror, Ent Ear, Nose, Throat Class 1 874.4420 1979-07-12
JEP Retainer, Matrix Dental Class 1 872.4565 1979-07-12

Official Correspondent

SIBYLLE SCHEPPERHEYN

US Agent Details

Yong Sun Business: EMERGO GLOBAL REPRESENTATION LLC Email: USAgent@UL.com Phone: (512) 3279997

Related Public Records

Same Entity

E. HAHNENKRATT 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
K831136 Almore Intl., Inc. DOUBLE BOW TOOTH SEPARATOR 1983-06-08

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8010445. Last updated year: 2026. Please use registration number 8010445 when referencing this establishment in official correspondence.
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