Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012889794

FEI Number

3012889794

Entity Name

LEEDS TEST OBJECTS LTD

City/State/Country

BOROUGHBRIDGE, YORK North Yorkshire, GB

Establishment Address

UNIT 9 BECKLANDS CLOSE, BOROUGHBRIDGE, YORK North Yorkshire YO51 9NR, GB

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

LEEDS TEST OBJECTS LTD (Owner Number: 10094586)

Owner / Operator Contact Address

UNIT 9 BECKLANDS CLOSE, BOROUGHBRIDGE, YORK, GB-NYK YO51 9NR, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Leeds Test Objects

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IXF	Test-Pattern, Radiographic	Radiology	Class 1	892.1940	2025-12-09

Official Correspondent

Adrian Walker

US Agent Details

Danny West Business: FDA Agent Pro LLC Email: dwest@fdaagentpro.com Phone: (619) 4103383

Related Public Records

Same Entity

LEEDS TEST OBJECTS LTD

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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3011168908	PRO-PROJECT	Okszow Lubuskie, PL
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012889794. Last updated year: 2026. Please use registration number 3012889794 when referencing this establishment in official correspondence.