Adentatec GmbH

FDA Device Registration & Listing · Woerth am Main Bavaria, DE · Registration 3010605319

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
3010605319
FEI Number
3010605319
Entity Name
Adentatec GmbH
City/State/Country
Woerth am Main Bavaria, DE
Establishment Address
Dr.-Konrad-Wiegand-Str. 9, Woerth am Main Bavaria 63939, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Adentatec GmbH (Owner Number: 10045442)
Owner / Operator Contact Address
Dr.-Konrad-Wiegand-Str. 9, Woerth am Main, DE-BY 63939, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

System Ti5-Blank System MG System Duro System KN System SIN System NH System Soft System NE System Soft Blank

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EJH Alloy, Metal, Base Dental Class 2 872.3710 2013-11-18

Official Correspondent

Julia Grabensee

US Agent Details

Jane Campbell Business: J & D Campbell Associates Inc. Email: jdcainc.sc@gmail.com Phone: (843) 3143670

Related Public Records

Same Entity

Adentatec 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
K810521 C.Vaupel Dental, Inc. CO-SPAN 13.5 CASTING ALLOY 1981-03-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010605319. Last updated year: 2026. Please use registration number 3010605319 when referencing this establishment in official correspondence.
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