Carpenter ENGINEERED FOAMS GERMANY GMBH

FDA Device Registration & Listing · Leverkusen North Rhine-Westphalia, DE · Registration 3009335681

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
3009335681
FEI Number
3009335681
Entity Name
Carpenter ENGINEERED FOAMS GERMANY GMBH
City/State/Country
Leverkusen North Rhine-Westphalia, DE
Establishment Address
Dieselstrasse 7, Leverkusen North Rhine-Westphalia 51381, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Carpenter Engineered Foams Germany GmbH (Owner Number: 10037948)
Owner / Operator Contact Address
Dieselstrasse 7, Leverkusen, DE-NW 51381, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FMP Protector, Skin Pressure General Hospital Class 1 880.6450 2026-04-23

Official Correspondent

Sven Koggel

US Agent Details

John Vins Business: Carpenter Americas, Inc. Email: john.vins@carpenter.com Phone: (864) 3507991

Related Public Records

Same Entity

Carpenter Engineered Foams Germany GmbH
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 3009335681. Last updated year: 2026. Please use registration number 3009335681 when referencing this establishment in official correspondence.
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