Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1000304307

FEI Number

1000304307

Entity Name

SCHEFTNER GMBH

City/State/Country

Mainz Rhineland-Palatinate, DE

Establishment Address

Dekan-Laist-Str. 52, Mainz Rhineland-Palatinate 55129, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Scheftner GmbH (Owner Number: 10048033)

Owner / Operator Contact Address

Dekan-Laist-Str. 52, Mainz, DE-NOTA 55129, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Starbond Ti4 Mogucera N Starbond CoS Mogucera C Starbond Easy Starbond Ti5 ModelStar S TiplaDur23 Starbond Co i-ProMelt Fusion AM

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EJH	Alloy, Metal, Base	Dental	Class 2	872.3710	2014-11-29

Official Correspondent

No official correspondent registered.

US Agent Details

Franz Menean Business: MEDAGENT Inc. Email: mail@medagent-usa.com Phone: (603) 5702039

Related Public Records

Same Entity

Scheftner 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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3010605319	Adentatec GmbH	Woerth am Main Bavaria, DE
3039443707	SHANGHAI FRONTIER MATERIAL TECH CO., LTD.	Shanghai, CN
2014676	The Belport Company, Inc DBA Gingi-Pak	CAMARILLO, CA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000304307. Last updated year: 2026. Please use registration number 1000304307 when referencing this establishment in official correspondence.