Waldemar Knittel Glasbearbeitungs GmbH

FDA Device Registration & Listing · BRAUNSCHWEIG, NIEDERSACHSEN Lower Saxony, DE · Registration 1000469910

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
1000469910
FEI Number
1000469910
Entity Name
Waldemar Knittel Glasbearbeitungs GmbH
City/State/Country
BRAUNSCHWEIG, NIEDERSACHSEN Lower Saxony, DE
Establishment Address
VARRENTRAPPSTRASSE 5, BRAUNSCHWEIG, NIEDERSACHSEN Lower Saxony 38114, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
KNITTEL GLAESER (Owner Number: 9042741)
Owner / Operator Contact Address
VARRENTRAPPSTRASSE 5, --, BRAUNSCHWEIG, NIEDERSACHSEN, DE-NOTA 38114, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Starfrost Alinity h-series Glass Slides

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KEW Slides, Microscope Pathology Class 1 864.3010 2000-08-28

Official Correspondent

No official correspondent registered.

US Agent Details

Antonio Lizarraga Business: StatLab Medical Products Email: ALizarraga@statlab.com Phone: (800) 4423573

Related Public Records

Same Entity

KNITTEL GLAESER
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000469910. Last updated year: 2026. Please use registration number 1000469910 when referencing this establishment in official correspondence.
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