SCHEU-DENTAL custom-made GmbH

FDA Device Registration & Listing · Hilden North Rhine-Westphalia, DE · Registration 3012859919

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
3012859919
FEI Number
3012859919
Entity Name
SCHEU-DENTAL custom-made GmbH
City/State/Country
Hilden North Rhine-Westphalia, DE
Establishment Address
Walder Strasse 53, Hilden North Rhine-Westphalia 40724, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SCHEU-DENTAL custom-made GmbH (Owner Number: 10052080)
Owner / Operator Contact Address
Walder Str. 53, Hilden, DE-NW 40724, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MEMOTAIN®, MEMOTAIN® Peek 3D

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DYJ Retainer, Screw Expansion, Orthodontic Dental Class 1 872.5410 2016-06-10

Official Correspondent

Alireza Assadi

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@ul.com Phone: (512) 3279997

Related Public Records

Same Entity

SCHEU-DENTAL custom-made GmbH
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012859919. Last updated year: 2026. Please use registration number 3012859919 when referencing this establishment in official correspondence.
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