EYEWEAR SOLUTION S GMBH

FDA Device Registration & Listing · Hartberg Steiermark, AT · Registration 3008598038

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
3008598038
FEI Number
3008598038
Entity Name
EYEWEAR SOLUTION S GMBH
City/State/Country
Hartberg Steiermark, AT
Establishment Address
Josef Hallamayerstrasse 62, Hartberg Steiermark 8230, AT
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
EYEWEAR SOLUTION S GmbH (Owner Number: 10039009)
Owner / Operator Contact Address
Josef Hallamayrstrasse 62, Hartberg, AT-6 8230, 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
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2011-12-02

Official Correspondent

Christian Krois

US Agent Details

Kela Veshi Business: Veshi Consulting Email: kelaveshi@yahoo.com Phone: (301) 7920964

Related Public Records

Same Entity

EYEWEAR SOLUTION S 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
K910951 United Optical, Spa OPTHLAMIC FRAMES 1991-05-06

Similar Registrations

Registration Number Establishment Name Location
3007521479 NY2LA INC. Camarillo, CA, US
3005147601 VISIONTECH EXPORT INTERNATIONAL (PVT) LTD. KARACHI Sindh, PK
3009554831 ROGER EYE DESIGN Etten-Leur Noord-Brabant, NL
3013507321 DEM FACTORY S.R.L. Limana Belluno, IT
3015243992 L.G.R SRL Roma, IT
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008598038. Last updated year: 2026. Please use registration number 3008598038 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.