Atritech, Inc.

Normedix, Inc.

Vascular Solutions, Inc.

Surmodics, Inc.

Angioguard, Inc.

Spectra Science Corporation

Boston Scientific Scimed, Inc.

Cordis Corporation

Merit Medical Systems, Inc.

Teleflex Life Sciences Pte. Ltd.

Urologix, Inc.

Contego Medical, LLC

Teleflex Innovations S.a.r.l.

Orthopaedic Innovations, Inc.

Teleflex Medical Devices S.a.r.l

Gregg Stuart Sutton

Jeffrey M Welch

Thomas E Borillo

Howard C Root

Jason M Garrity

Robert G Hauser

David Holmes

Robert A VanTassel

Karl V Ganske

Robert Schwartz

Eric Joseph Dille

Dean A Peterson

John Bridgeman

Jeffery Foster Larson

Francis C Peterson

James Arnold Murto

Stephen Anthony Penegor

Wesley D Johnson

Brian T McMahon

Bruce Wayne Stursa

Bruce R Youngberg

James V Kauphusman

Brian W Stevens

Joram Slager

Jay Yadav

Ravish Sachar

Christopher J Clark

Jonathan L Flachman

Jonathan R McGrath

Steve Michael

Charles Olson

Larry A Roberts

Mark Maciejewski

Amy Raatikka

Amy Trocke

Thomas Borillo

James Murto

Stephen Penegor

Jay S Yadav

A catheter assembly includes a catheter body extending from a catheter proximal portion to a catheter distal portion. The catheter body includes an inner liner and an outer sleeve. A braid assembly is within the catheter body and between the inner liner and the outer sleeve. The braid assembly includes a first filar array including one or more first filars helically extending around the catheter body in a first direction. The braid assembly further includes a second filar array including one or more second filars helically extending around the catheter body in a second direction opposed to the first direction.

Braided catheter assemblies

Embodiments include an interventional guide catheter, comprising: a main tubular shaft with a distal tip and proximal end; the main tubular shaft comprising: a main inner structural layer comprising a metallic helically wound multi-filar wire extending from a proximal tube termination to a distal end, a braided wire layer covering the main inner structural layer that extends from the proximal tube termination to the distal end, an outer layer of polymer jacketing fixedly attached to the main inner structural layer and braid layer, an inner layer of polymer jacketing and fixedly attached to the main inner structural layer, a distal tip made of layers of polymer, a distal end curve shape for anatomical conformance that is heat processed in the main metal portion of the structure; and a lamination of the inner layer, main inner structural layer, braided wire layer and outer layer. Other embodiments are also included herein.

Coronary guide catheter

An anchored dilator includes a push tube having proximal and distal push tube portions. A dilator tip is coupled with the distal push tube portion and is configured for selectable coupling with a catheter. The dilator tip includes an anchor cuff having a cuff interface. The anchor cuff is configured to transition between a shuttle configuration having a shuttle profile and an anchored configuration having an anchored profile larger than the shuttle profile. A cuff operator assembly is configured to transition the anchor cuff between the anchored and shuttle configurations. The cuff operator assembly includes a cuff operator movably coupled with the dilator tip, and an operator shaft coupled with the cuff operator. The operator shaft extends toward the proximal push tube portion. Actuation of the cuff operator with the operator shaft transitions the anchor cuff between the shuttle configuration and the anchored configuration.

Anchored dilator system and methods for same

The present technology relates to a hemostasis sealing device having a device enclosure with a first seal portion for a medical device and a second seal portion for guide wire sealing. The device enclosure can be generally configured for compressive communication with a housing. The second seal portion can define a split that is in compressive communication with structural elements of the hemostasis sealing device, which can simultaneously provide sealing functionality and allow passage of relatively large-bore devices.

Hemostasis sealing device

The disclosure provides insertion tools and articles that facilitate entry of a medical device, such as a balloon catheter, into the body, and that can provide advantages in terms of balloon insertion, safety, and drug delivery. The insertion tool includes a tubular portion that accommodates a balloon portion of a balloon catheter, and one or more separation margin(s) in the wall of the tubular portion or one or more split(s) in the tubular wall. The insertion tool also includes a proximal tab that extends from a second lengthwise half having a portion at an angle skew to the lengthwise axis, or that is in the form of a solid article comprising a concave surface that is fastened to an outer surface of the second lengthwise half of the tubular portion; or first and second tabs that extend from first and second lengthwise halves of the tubular portion, respectively.

Lubricious insertion tools for medical devices and methods for using

Embodiments of the invention include a multi-lumen catheter for extracting or aspirating a blood clot or thrombus from arterial or veinous sites. Other embodiments are also included herein.

Thrombus extraction catheter

Embodiments of the invention include an introducer for introducing interventional catheters into the vasculature comprising a distal tip, a proximal end, a structural layer, an inner layer, and an outer layer. Other embodiments are also included herein.

Introducer sheath for radial artery access

Apparatus for permanent placement across an ostium of a left atrial appendage in a patient, which includes a filtering membrane configured to extend across the ostium of the left atrial appendage. The filtering membrane has a permeable structure which allows blood to flow through but substantially inhibits thrombus from passing therethrough. The apparatus also includes a support structure attached to the filtering membrane which retains the filtering membrane in position across the ostium of the left atrial appendage by permanently engaging a portion of the interior wall of the left atrial appendage. The support structure may be radially expandable from a first configuration to a second configuration which engages the ostium or the interior wall of the left atrial appendage. The filtering membrane may define an opening therethrough that is configured to expand from a first size which inhibits the passage of thrombus therethrough to a second size which allows an interventional device, e.g., an expansion balloon, to pass therethrough, and wherein the opening is resiliently biased towards the first size.

Filter apparatus for ostium of left atrial appendage

Catheters and methods for supporting a guidewire or delivering a radiopaque, diagnostic or therapeutic agent through a vessel stenosis or other tortuous anatomy are disclosed. A catheter can comprise an elongate shaft body and a tip member disposed at a distal end of the shaft body. The shaft body can extend from a proximal end to the distal end and can define an inner lumen. The shaft body can include a liner, a braid member surrounding the liner, a multi-layer coil surrounding the braid member, and a polymer cover surrounding the multi-layer coil. The multi-layer coil can include first and second coil layers wound in opposing directions. An outer surface portion of the polymer cover can include one or more helical threads. In an example, the one or more helical threads are positioned around a distal end portion of the shaft body. The tip member can be made from a metal or a polymer and can also include one or more helical threads around its outer surface.

Catheter

Instrumentation for percutaneous delivery of blood filtration devices to atrial appendages includes a curved access sheath and a delivery tube. A compressed filter device attached to a tether wire is loaded in the delivery tube. The access sheath and the delivery tube can be mechanically locked and moved together to place the device in a suitable deployment position. The device is deployed by expelling it from the delivery tube either by retracting the delivery tube over the tether wire, or by moving the tether wire forward through the delivery tube. A filter membrane in the deployed device extends across the appendage ostium to filter blood flow through the ostium. The filter membrane is configured to present a flat surface to atrial blood flow past the ostium.

Atrial appendage blood filtration systems

The invention being disclosed describes a medical device for removal of a thrombus or clot in a vascular setting by using a rotational, expandable basket structure in combination with drug infusion, blood/particle aspiration and clot isolation by distal and proximal occlusion.

Clot removal device for deep vein thrombosis

Clot removal device for blood vessels

Growing community of inventors

Maple Grove, MN, United States of America

Gregg Stuart Sutton