LUKAS-ERZETT GMBH & CO. KG

FDA Device Registration & Listing · Engelskirchen North Rhine-Westphalia, DE · Registration 3013247796

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
3013247796
FEI Number
3013247796
Entity Name
LUKAS-ERZETT GMBH & CO. KG
City/State/Country
Engelskirchen North Rhine-Westphalia, DE
Establishment Address
Gebrueder-Lukas-Strasse 1, Engelskirchen North Rhine-Westphalia 51766, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
LUKAS-ERZETT GmbH & Co. KG (Owner Number: 10093321)
Owner / Operator Contact Address
Gebrueder-Lukas-Strasse 1, Engelskirchen, DE-NW 51766, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

GT-SPECIAL SK-PODO SK-THERMO GT-PODO

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GFF Bur, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4820 2025-04-29

Official Correspondent

Axel Schmidt

US Agent Details

Barbara Fisher Business: Johner Institute North America Email: us-agent@johner-institut.com Phone: (301) 2446335

Related Public Records

Same Entity

LUKAS-ERZETT GmbH & Co. KG
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 3013247796. Last updated year: 2026. Please use registration number 3013247796 when referencing this establishment in official correspondence.
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