Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008352701

FEI Number

3008352701

Entity Name

KLINIKA MEDICAL GMBH

City/State/Country

Usingen Hesse, DE

Establishment Address

Am Dornbusch 29, Usingen Hesse 61250, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Klinika Medical GmbH (Owner Number: 10032108)

Owner / Operator Contact Address

Am Dornbusch 29, Usingen, DE-HE 61250, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

KliniTray KliniTray

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NNI	Container, Specimen, Non-Sterile	Pathology	Class 1	864.3250	2010-04-09
FMH	Container, Specimen, Sterile	Pathology	Class 1	864.3250	2010-04-09

Official Correspondent

Sylvia Katzke

US Agent Details

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

Related Public Records

Same Entity

Klinika Medical 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 3008352701. Last updated year: 2026. Please use registration number 3008352701 when referencing this establishment in official correspondence.