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USPTO Patent Application: Non-occluding Balloon Catheter for Cardiovascular Drug Delivery

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Published December 1st, 2025
Detected March 26th, 2026
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Summary

The USPTO has published a patent application for a non-occluding balloon catheter device designed for cardiovascular drug delivery. The application details a device that allows blood flow to continue through a bypass lumen while a drug coating is applied to the vessel wall. This innovation aims to improve drug delivery efficacy in cardiovascular treatments.

What changed

This document is a USPTO patent application (US20260083942A1) filed on December 1, 2025, for a novel non-occluding balloon catheter device intended for cardiovascular drug delivery. The device features a bypass lumen that ensures continued blood flow when the balloon is inflated, while simultaneously pressing a drug coating against the blood vessel wall. The abstract highlights the dual functionality of maintaining blood transport and delivering therapeutic agents.

This patent application represents a new technological development in the medical device and pharmaceutical sectors. While it does not impose immediate compliance obligations, it signals potential future innovations in drug-eluting balloon technology. Companies involved in cardiovascular devices, drug coatings, and interventional cardiology should monitor patent filings in this area for competitive intelligence and potential licensing opportunities. No specific compliance deadlines or penalties are associated with a patent application itself.

Source document (simplified)

← USPTO Patent Applications

NON-OCCLUDING BALLOON FOR CARDIOVASCULAR DRUG DELIVERY

Application US20260083942A1 Kind: A1 Mar 26, 2026

Inventors

Vijay Sitharam Ramanath, Brett Allyn Williams

Abstract

A non-occluding drug-coated balloon catheter device for use in a blood vessel transporting blood comprises a catheter shaft including a guidewire lumen, a fluid lumen and a connector port. A balloon is mounted on the catheter shaft and includes an outer envelope surrounding the guidewire lumen in fluid communication with the fluid lumen; a drug coating applied on the exterior surface of the outer envelope; and at least one bypass lumen forming a passage extending from the proximal end of the outer envelope to the distal end of the outer envelope. When the balloon is positioned in a blood vessel and inflated, the exterior surface of the outer envelope presses the drug coating against the blood vessel and the bypass lumen is open between the distal end of the outer envelope and the proximal end of the outer envelope such that blood transport continues through the bypass lumen.

CPC Classifications

A61M 25/10 A61M 25/1029 A61M 25/104 A61M 2025/0183 A61M 2025/105 A61M 2025/1072 A61M 2025/1075 A61M 2025/1079 A61M 2025/1086 A61M 2025/1097

Filing Date

2025-12-01

Application No.

19404950

View original document →

Named provisions

Abstract

Source

Analysis generated by AI. Source diff and links are from the original.

Classification

Agency
USPTO
Published
December 1st, 2025
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
US20260083942A1

Who this affects

Applies to
Drug manufacturers Medical device makers Pharmaceutical companies
Industry sector
3254 Pharmaceutical Manufacturing 3345 Medical Device Manufacturing
Activity scope
Drug Delivery
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Product Development
Topics
Medical Devices Pharmaceuticals

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