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USPTO Patent Grant: Durability and Particulate Testing System

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Summary

The USPTO has granted patent US12582523B1 for a durability and particulate testing system and method for medical devices. The patent, assigned to DYNATEK LABS, INC., details a system for simulating the expected lifetime of synthetic structural heart devices.

Published by USPTO on changeflow.com . Detected, standardized, and enriched by GovPing. Review our methodology and editorial standards .

What changed

The United States Patent and Trademark Office (USPTO) has granted patent US12582523B1, titled "Durability and particulate testing system and method," to DYNATEK LABS, INC. The patent covers a system designed for testing the durability and particulate generation of medical devices, particularly synthetic structural heart devices. Key components include a durability tester, simulated blood fluid, fluid lines, a particle counter, flow meters, a fluid management system, and system controllers with software for operation and data recording. Some embodiments include temperature control to simulate physiological conditions.

This patent grant is primarily an intellectual property matter and does not impose direct regulatory obligations on medical device manufacturers. However, it signifies a novel technological advancement in product testing. Companies involved in the development or testing of cardiovascular devices may wish to review the patent claims to ensure their own testing methodologies do not infringe upon this granted patent. The filing date was April 11, 2023, and the patent is set to be granted on March 24, 2026.

Archived snapshot

Mar 24, 2026

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← USPTO Patent Grants

Durability and particulate testing system and method

Grant US12582523B1 Kind: B1 Mar 24, 2026

Assignee

DYNATEK LABS, INC.

Inventors

Christopher Conti, James Conti, Alicia Sullivan, Donald Rohde, Kendra Conti, Elaine Strope

Abstract

A medical device durability and particulate testing system is provided including a durability tester component configured for continually actuating movement of structural device(s); a simulated blood fluid; fluid flow lines; a particle counter component configured for recording continuous particulate data from device(s) subjected to durability testing; flow meters; a fluid management system; and one or more system controller(s) having a processor configured with software for controlling operation of the system and recording data. In an embodiment, the system includes a user interface accessible via a display. In some embodiments the system further includes a heater paired with temperature measuring devices to maintain fluid temperatures within appropriate bounds to simulate blood within the body. In an exemplary embodiment, the durability and particulate testing system is a continuous flow, closed loop system and configured for testing synthetic structural heart devices to simulate the expected lifetime of the device(s).

CPC Classifications

A61F 2/2472 A61F 2240/008 G01N 3/567 G01N 15/0618

Filing Date

2023-04-11

Application No.

18133406

Claims

20

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Named provisions

Abstract Claims

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Last updated

Classification

Agency
USPTO
Published
March 24th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
US12582523B1

Who this affects

Applies to
Drug manufacturers Medical device makers
Industry sector
3345 Medical Device Manufacturing
Activity scope
Product Testing Medical Device Development
Geographic scope
United States US

Taxonomy

Primary area
Medical Devices
Operational domain
Research & Development
Topics
Product Testing Intellectual Property

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