TWE DIERDORF GMBH AND CO. KG

FDA Device Registration & Listing · Dierdorf Rhineland-Palatinate, DE · Registration 3014425119

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
3014425119
FEI Number
3014425119
Entity Name
TWE DIERDORF GMBH AND CO. KG
City/State/Country
Dierdorf Rhineland-Palatinate, DE
Establishment Address
Poststrasse 29, Dierdorf Rhineland-Palatinate 56269, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
TWE Dierdorf GmbH and Co. KG (Owner Number: 10057318)
Owner / Operator Contact Address
Poststrasse 29, Dierdorf, DE-RP 56269, 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
ITG Bandage, Cast Physical Medicine Class 1 890.3025 2018-03-21

Official Correspondent

No official correspondent registered.

US Agent Details

Sam Shaffer Business: L&R USA INC. Email: sam.shaffer@us.LRmed.com Phone: (414) 8924157

Related Public Records

Same Entity

TWE Dierdorf GmbH and Co. KG
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014425119. Last updated year: 2026. Please use registration number 3014425119 when referencing this establishment in official correspondence.
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