Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011168908

FEI Number

3011168908

Entity Name

PRO-PROJECT

City/State/Country

Okszow Lubuskie, PL

Establishment Address

Kwiatowa 43A, Okszow Lubuskie 22-105, PL

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

Pro-Project (Owner Number: 10050353)

Owner / Operator Contact Address

Kwiatowa 43A, Okszow, PL-08 22-105, PL

Initial Importer Flag

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
IXF	Test-Pattern, Radiographic	Radiology	Class 1	892.1940	2015-11-08

Official Correspondent

Rafal Kartaszynski

US Agent Details

Rafal Henryk Kartaszynski Business: Pro-Project LLC Email: contact.us@pro-project.pl Phone: (786) 7570514

Related Public Records

Same Entity

Pro-Project

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
K865100	Computerized Imaging Reference Systems, Inc.	TISSUE-EQUIVALENT BREAST SIMULATOR	1987-01-12

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3012889794	LEEDS TEST OBJECTS LTD	BOROUGHBRIDGE, YORK North Yorkshire, GB
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011168908. Last updated year: 2026. Please use registration number 3011168908 when referencing this establishment in official correspondence.