LUNOR Aktiengesellschaft

FDA Device Registration & Listing · Bad Liebenzell Baden-Wurttemberg, DE · Registration 9680301

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
9680301
FEI Number
3005447474
Entity Name
LUNOR Aktiengesellschaft
City/State/Country
Bad Liebenzell Baden-Wurttemberg, DE
Establishment Address
Lunor Allee 1, Bad Liebenzell Baden-Wurttemberg 75378, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Lunor AG (Owner Number: 10030562)
Owner / Operator Contact Address
Lunor Allee 1, Bad Liebenzell, DE-BW 75378, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

LUNOR Lunova Lunor

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2011-04-19
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2009-10-19

Official Correspondent

Michael Fux

US Agent Details

Donna Minthorn Business: Luxury Optical Holdings Email: dminthorn@loholdings.com Phone: (646) 7792897

Related Public Records

Same Entity

Lunor AG
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
K940726 Jay-Y Enterprises Co., Inc. NONE-GENERIC 1994-04-11
K934837 Simon Marketing, Inc. SUNGLASSES 1993-12-08
K852902 Yours Enterprise Co., Ltd. METALLIC SUNGLASSES 1985-08-12
K970895 Custom Optical Frames, Inc. CUSTOM OPTICAL SUNGLASS FRAMES 1997-05-06
K853921 Winsburn Company , Ltd. ALL KINDS OF SUNGLASSES 1985-10-15

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9680301. Last updated year: 2026. Please use registration number 9680301 when referencing this establishment in official correspondence.
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