ORGREEN OPTICS APS.

FDA Device Registration & Listing · COPENHAGEN Hovedstaden, DK · Registration 3005552045

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
3005552045
FEI Number
3005552045
Entity Name
ORGREEN OPTICS APS.
City/State/Country
COPENHAGEN Hovedstaden, DK
Establishment Address
Overgade Oven Vandet 58a, 1st Floor, COPENHAGEN Hovedstaden 1415, DK
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
ORGREEN OPTICS APS. (Owner Number: 9083407)
Owner / Operator Contact Address
Overgade Oven Vandet 58a, 1st Floor, COPENHAGEN, DK-85 1415, DK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Orgreen Optics APS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2006-02-24

Official Correspondent

No official correspondent registered.

US Agent Details

Morten Hansen Business: Orgreen Goldsmith LLC Email: mh@orgreenoptics.com Phone: (510) 9840082

Related Public Records

Same Entity

ORGREEN OPTICS APS.
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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005552045. Last updated year: 2026. Please use registration number 3005552045 when referencing this establishment in official correspondence.
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