EC Certification Service GmbH

FDA Device Registration & Listing · St. Veit/Glan Karnten, AT · Registration 3008796797

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
3008796797
FEI Number
3008796797
Entity Name
EC Certification Service GmbH
City/State/Country
St. Veit/Glan Karnten, AT
Establishment Address
Sandgasse 39a, St. Veit/Glan Karnten 9300, AT
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
EC Certification Service GmbH (Owner Number: 10035465)
Owner / Operator Contact Address
Sandgasse 39a, St. Veit/Glan, AT-2 9300, AT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DZC Wire, Orthodontic Dental Class 1 872.5410 2022-12-30

Official Correspondent

Elisabeth Moschik

US Agent Details

Rutledge Reynolds Email: rutreynolds@prrortho.com Phone: (214) 2323122

Related Public Records

Same Entity

EC Certification Service 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
K112640 Ormco Corp. HYPERELASTIC WIRE 2011-11-16

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008796797. Last updated year: 2026. Please use registration number 3008796797 when referencing this establishment in official correspondence.
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