Cook Medical Technologies LLC

Vance Products Inc.

Cook Ireland Limited

Electromedical Associates, LLC

Lithotech Medical, Limited

Cook Incorporated

Shay Joseph Lavelle

Paul David Devereux

John Neilan

Kenneth C Kennedy, Ii

Michael S Clancy

Gerard Treacy

James Butler

Michael Ryan

James M Carlson

Alison Liddy

Syed Ansar Md Tofail

Donncha Haverty

Shane Carr

Tim McGloughlin

Fionán Keady

Robert Allen Van Wyk

Frank J Fischer, Jr

Yuval Carmel

Anatoly Shkvarunets

Valery Diamant

Fionan Keady

James Giltinan

Ger Houlihan

Walter N Ryan

Marvin O Andrews

Nadezda Yasko

Stepan Khachin

Vladimir Khachin

Jessica Watts Miller

Tatjana Dutova

Arthur Thomas Henry

Therese Fitzgibbon

Patrick Martin Kelly

Tim Mcgloughlin

Paul Devereaux

Syed Ansar Tofail

Vincent Mchugo

Kenneth C Kennedy

A single-wire stylet may be constructed as an elongate single-wire, memory-metal alloy body with a generally cylindrical body profile, extending distally from a proximal end terminus, where embodiments include a polymeric distal tip member fixedly attached directly at a distal end of the single-wire body. At least one lengthwise portion of the single-wire body is at least partially in martensitic phase at operating temperatures at and below about 37&#xb0; C. Where present, the polymeric distal tip member has a generally cylindrical body profile circumferentially bounded by an outer circumference substantially equal to or greater than that of the metal body. The polymeric distal tip member may be overmolded upon a distal-end tip length of an elongate single-wire, memory-metal alloy stylet body, where the distal end and/or discrete intermediate distal-portion length(s) that include martensitic-phase alloy and any polymeric member have greater flexibility than a proximal-most length of the alloy stylet body.

Endoscopic needle stylet with enhanced-flexibility lengths

Embodiments include a fiducial deployment system. A fiducial may include dimples to enhance echogenicity and/or to provide for engagement with a delivery cannula or stylet. The needle system may be configured to deliver a plurality of fiducials to a target location in serial fashion, one at a time, when the fiducials are coaxially disposed around a central deployment member that may be embodied as a delivery cannula or stylet. In certain embodiments, echogenic placement of fiducials may present certain advantages. An elongate structure may be included that is configured to distally advance fiducials along the deployment member.

Fiducial deployment needle system

A prosthesis and a method of manufacturing the prosthesis for controlling flow through a bodily lumen are provided. The prosthesis includes a body having a proximal portion, a distal portion and a lumen extending therethrough. The prosthesis also includes a valve operably connected to the body. The valve has a proximal portion, a distal portion and a lumen extending through the valve, where the valve lumen is connected to the body lumen. The valve is configured to be closed in the absence of an antegrade pressure and a retrograde pressure, the retrograde pressure being greater than the antegrade pressure. The valve includes a material portion operably connected to the valve, the material portion providing increased stiffness to the valve relative to the valve alone, wherein the material portion is configured to facilitate self-reversion of the valve to the closed configuration.

Anti-aspiration prosthesis

Disclosed herein are embodiments of an electrosurgical device that include one or more floating electrodes and are specifically adapted to remove, resect, ablate, vaporize, denaturize, coagulate and form lesions in soft tissues, preferably in combination with a resectoscope, particularly in the context of urological, gynecological, laparoscopic, arthroscopic, and ENT procedures. Specific adaptations for urological and gynecological applications, for example BPH treatment, are also described.

Plasma resection electrode

Disclosed herein is a nickel-titanium alloy comprising nickel, titanium, and at least one rare earth element. The nickel-titanium alloy comprises from about 34 at. % to about 60 at. % nickel, from about 34 at. % to about 60 at. % titanium, and from about 0.1 at. % to about 15 at. % at least one rare earth element. The nickel-titanium alloy may further include one or more additional alloying elements. In addition to radiopacity, the nickel-titanium alloy preferably exhibits superelastic or shape memory behavior. Medical devices comprising the nickel-titanium alloy and a method of making them are also disclosed.

Nickel-titanium alloy including a rare earth element

A handle for receiving an elongate medical device is provided. The handle includes a housing defining an elongate hollow interior portion, the hollow portion defining a first portion proximate the distal end and the aperture, a second portion. A core is slidably disposed within the interior portion and includes a ramp portion extending from an outer surface of the core at an oblique angle to the longitudinal axis, and two or more arms extending outwardly from a proximal end of the core and biased toward an extended configuration where a proximal end of each arm extends radially outside of an outer surface of the core, wherein the two or more arms combine to define the proximal opening. A button is movably disposed within the aperture substantially blocking communication with the hollow portion through the aperture, comprising an inclined surface that slidably engages the ramp surface.

Button release handle

A stent is provided. The stent includes an elongate body comprising a tightly coiled wire disposed therealong, the coiled wire spanning between a first end portion and a second end portion, and defining a lumen therethrough. A safety wire is disposed through the lumen and fixed with respect to each of the first and second end portions. Proximal and distal end caps are fixed to the ends of the safety wire. At least one of the proximal and distal end caps comprises a window configured to receive the safety wire therethrough, and configured to allow access to the safety wire to weld the safety wire and the respective end cap.

Flexible stent and delivery system

A medical device with an outer surface prepared to reduce crystalline growth or surface fowling thereon is provided. The device includes an elongate member that extends between a distal end and a proximal end, and a lumen defined through at least a central portion of the member. The member is defined from a wire that is coiled to define the lumen therethrough, the coils of the wire are configured such that a plurality of the neighboring coils define a small space therebetween. The coiled wire includes a central metallic core that extends along the entire length of the wire defining the member and a polymeric jacket is wrapped around the core, wherein the polymeric jacket is configured to retain an electric charge disposed therethrough.

Electrically charged medical device

Devices are illustrated which provide for accurately controlling the extension of a needle from a protective sheath to increase accuracy and improve the outcome of the treatment procedure.

Apparatus for accurately controlling needle extension

Growing community of inventors

County Limerick, Ireland

Shay Joseph Lavelle