DIETZ GMBH

FDA Device Registration & Listing · Karlsbad Baden-Wurttemberg, DE · Registration 3006440543

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
3006440543
FEI Number
3006440543
Entity Name
DIETZ GMBH
City/State/Country
Karlsbad Baden-Wurttemberg, DE
Establishment Address
Reutackerstrasse 12, Karlsbad Baden-Wurttemberg 76307, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Dietz GmbH (Owner Number: 10089963)
Owner / Operator Contact Address
Reutackerstrasse 12, Karlsbad, DE-NOTA 76307, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Homecraft XL Bathmaster KANJO XL KANJO B-protect KANJO turning aid KANJO Eco Bathlift Bathmaster Deltis Bathmaster Deltis Bathmaster XL Bathmaster by Homecraft Bathmaster Sonaris KANJO Power turning and transfer aid KANJO, KANJO POWER, KANJO ECO, KANJO B-Protect, KANJO XL, Bathmaster deltis, Sonaris, Katnic

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FNG Lift, Patient, Ac-Powered General Hospital Class 2 880.5500 2025-12-09
INN Chair, Adjustable, Mechanical Physical Medicine Class 1 890.3100 2024-01-26

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K912769 Century Manufacturing Co. PATIENT LIFT AND TRANSPORT 1991-10-02

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006440543. Last updated year: 2026. Please use registration number 3006440543 when referencing this establishment in official correspondence.
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