Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015131021

FEI Number

3015131021

Entity Name

SCHOEPF FERTIGUNGSTECHNIK GMBH

City/State/Country

Bludesch Vorarlberg, AT

Establishment Address

Hauptstrasse 65, Bludesch Vorarlberg 6719, AT

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SCHOEPF Fertigungstechnik GmbH (Owner Number: 10059219)

Owner / Operator Contact Address

Hauptstrasse 65, Bludesch, AT-8 6719, AT

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Articulator CA 3

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EJP	Articulators	Dental	Class 1	872.3150	2018-12-17

Official Correspondent

Thomas Schoepf

US Agent Details

Peter Hasslacher Business: Austrian Trade Commissioner Email: NewYork@advantageaustria.org Phone: (212) 4215250

Related Public Records

Same Entity

SCHOEPF Fertigungstechnik GmbH

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 3015131021. Last updated year: 2026. Please use registration number 3015131021 when referencing this establishment in official correspondence.