WALZ ELEKTRONIK GMBH

FDA Device Registration & Listing · Rohrdorf Baden-Wurttemberg, DE · Registration 1000161819

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
1000161819
FEI Number
1000161819
Entity Name
WALZ ELEKTRONIK GMBH
City/State/Country
Rohrdorf Baden-Wurttemberg, DE
Establishment Address
Walddorfer Strasse 40, Rohrdorf Baden-Wurttemberg 72229, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Walz Elektronik GmbH (Owner Number: 10088634)
Owner / Operator Contact Address
Walddorfer Strasse 40, Rohrdorf, DE-BW 72229, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K230488
PMA Number
N/A

All Registered Proprietary Names

electrohydraulic Lithotriptor sterile EHL-Probes

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FFK Lithotriptor, Electro-Hydraulic Gastroenterology, Urology Class 2 876.4480 2023-09-11

Official Correspondent

Christian Schweizer

US Agent Details

German American Chamber of Commerce, Inc. German American Ch Email: legalservices@gaccny.com Phone: (212) 9748830

Related Public Records

Same Entity

Walz Elektronik 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
K885255 Candela Laser Corp. MDL-1 LASERTRIPTER(TM) 1989-06-01

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000161819. Last updated year: 2026. Please use registration number 1000161819 when referencing this establishment in official correspondence.
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