WALDMANN LIGHTING

FDA Device Registration & Listing · Wheeling, IL, US · Registration 1000279762

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
1000279762
FEI Number
1000279762
Entity Name
WALDMANN LIGHTING
City/State/Country
Wheeling, IL, US
Establishment Address
9 WEST CENTURY DRIVE, Wheeling, IL 60090, US
Establishment Type(s)
Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
HERBERT WALDMANN GMBH & CO. (Owner Number: 8010699)
Owner / Operator Contact Address
9 W Century Dr, Wheeling, IL 60090, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Multiple WLA Multiple Taneo Multiple Omnivue Multiple Halux N30 Multiple Visiano 10-1 Multiple Navigator Multiple Polaris Multiple Triango 30 Multiple ALD Multiple Visiano 20-2 Multiple Halux III Multiple Crescent Multiple Opticlux Multiple MLD Multiple TR7 Multiple Amadea Multiple Stellar Duo Multiple Halux N50 Multiple Stellar Multiple Triango 80 Multiple Tevisio Multiple Halux I Multiple Zera Multiple Triango 100

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KZF Device, Medical Examination, Ac Powered General Hospital Class 1 880.6320 2005-11-01

Official Correspondent

LES KAMINSKI

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

HERBERT WALDMANN GMBH & CO.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
1000312377 Derungs Licht AG Gossau Sankt Gallen, CH

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K851742 Burton Medical Products Corp. MEDICAL EXAMINATION LIGHTS 1985-05-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000279762. Last updated year: 2026. Please use registration number 1000279762 when referencing this establishment in official correspondence.
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