HOPF, RINGLEB & CO. GMBH & CIE.

FDA Device Registration & Listing · BERLIN, DE · Registration 9614987

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
9614987
FEI Number
5468
Entity Name
HOPF, RINGLEB & CO. GMBH & CIE.
City/State/Country
BERLIN, DE
Establishment Address
82 GARDESCHUETZENWEG, BERLIN D-12203, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
HOPF, RINGLEB & CO. GMBH & CIE. (Owner Number: 9031768)
Owner / Operator Contact Address
82 GARDESCHUETZENWEG, --, BERLIN, DE-NOTA D-12203, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

HORICO DIAMOND INSTRUMENT HORICO HORICO

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EHM Strip, Polishing Agent Dental Class 1 872.6010 1998-01-21
DZP Instrument, Diamond, Dental Dental Class 1 872.4535 1997-10-01
EHL Point, Abrasive Dental Class 1 872.6010 1998-01-21
EJL Bur, Dental Dental Class 1 872.3240 1998-01-21

Official Correspondent

Sonja Hopf-Heller

US Agent Details

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

Related Public Records

Same Entity

HOPF, RINGLEB & CO. GMBH & CIE.
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 9614987. Last updated year: 2026. Please use registration number 9614987 when referencing this establishment in official correspondence.
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