DR. HOPF GMBH & CO. KG

FDA Device Registration & Listing · LANGENHAGEN Lower Saxony, DE · Registration 8043621

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
8043621
FEI Number
3002781873
Entity Name
DR. HOPF GMBH & CO. KG
City/State/Country
LANGENHAGEN Lower Saxony, DE
Establishment Address
BAYERNSTRASSE 9, LANGENHAGEN Lower Saxony 30855, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
DR. HOPF GMBH & CO. KG (Owner Number: 9002748)
Owner / Operator Contact Address
Bayernstr. 9, Langenhagen, DE-NI D-30855, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SUNSHINE DIAMONDS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DZP Instrument, Diamond, Dental Dental Class 1 872.4535 1991-03-12
EJL Bur, Dental Dental Class 1 872.3240 2001-08-13
EHJ Disk, Abrasive Dental Class 1 872.6010 2001-08-13
EHL Point, Abrasive Dental Class 1 872.6010 2001-08-13

Official Correspondent

Felix Heller

US Agent Details

Gregory Pfingst Business: Pfingst & Co Inc. Email: sales@pfingstco.com Phone: (908) 5616400

Related Public Records

Same Entity

DR. HOPF 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 8043621. Last updated year: 2026. Please use registration number 8043621 when referencing this establishment in official correspondence.
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