Boston Scientific Scimed, Inc.

Scimed Life Systems, Inc.

Gyrus Acmi, Inc.

Other

Teleflex Life Sciences Pte. Ltd.

Vascular Solutions, Inc.

Gyms Acmi, Inc.

Gyros Acmi, Inc.

Scimed

Teleflex Innovation S.à.r.l.

Boston Scientific Corporation

Gyrus Acmi, Inc. (d.b.a. Olympus Surgical Technologies America)

Thomas J Holman

Jan Weber

Paul J Buscemi

Afsar Ali

Scott Schewe

Gregory K Olson

Fertac Bilge

Richard Dunn

Darlene A Thometz

David H Donabedian

Louis G Ellis

Nikhil M Murdeshwar

Judy Lin Walish

Scott M Hanson

Hui Tang

Richard J Traxler

Tracee E Eidenschink

Tracee E J Eidenschink

John Jianhua Chen

Liliana Atanasoska

Kemal Schankereli

Linda R Lorentzen Cornelius

James Lee Shippy, Iii

Hans G Mische

Danney Langanki

Joseph Huebsch

Lixiao Wang

Chad John Kugler

Daniel James Horn

Kurt G Shelton

Jeffrey S Lindquist

Robert Warner

Leo M Klisch

Sew-Wah Tay

Ken Xiao Kang Zhang

Peter Jacobs

Kevin Silberg

Nam H Hoang

David Parsons

Sonja J K Williams

Daniel M Lafontaine

Daniel O Adams

Riyad Moe

Matthew Charles Heidner

Roger Noel Hastings

Yousef F Alkhatib

Zachary J Tegels

Joey Magno

Richard J Olson

Daniel Keith Tomaschko

Scott P Thome

William H Penny

Jan D Seppala

Donald F Palme, Ii

Dale F Schmaltz

Nie Tang

Bradley C Linden

Joseph M Lyver

Steve Hoff

Linda Lorentzen Cornelius

Sew Wah Tay

David Griswold

Todd Allen Berg

Martin R Willard

Zane R Ward

David Bryan Robinson

John Mensch

David John Sogard

Howard C Root

Kent David Harrison

Richard L Goodin

Theodore C Blus

Henry John Pepin

Scott A Olson

Steven Paul Mertens

David J Serdar

Gary L Hendrickson

Joel M Wasdyke

Matthew J Miller

Michael Sansoucy

Fernando DiCaprio

Barry J O'Brien

Richard A Noddin

Ying Xiong

Hanam Sota Pham

Kristi Mae Flury

John E Arnold, Jr

Jeffrey D Holton

The Thomas Trinh Tran

Larry A Walter

Dan Quillin

Justin Plessel

Peter J Crowley

David J Haskvitz

Zach Tegels

James Heggestuen

Stacie Depner

Gina L Sandvick

Doug Fraser

Deepa Deepa

Closure systems, kits and methods for sealing a percutaneous puncture or other opening in a blood vessel wall, body cavity or biopsy tract are disclosed. A closure system can comprise an implant assembly, a delivery assembly, and an introducer sheath. The closure system can further comprise a valve bypass and a dilator. The implant assembly can include an inner member, a sealing membrane, and an outer member, each of which can be delivered by the delivery assembly. The inner member can be extended through the puncture or opening and positioned adjacent an inner tissue surface. The outer member can be positioned adjacent an outer tissue surface. The sealing membrane can have a distal end attached to the inner member, a proximal end including an opening configured to receive the outer member, and a mid-region therebetween. The outer member, when expanded from a delivery configuration to a sealing configuration, can urge the mid-region of the sealing membrane radially outward such that its outer surface can contact and conform to a perimeter edge of the puncture or opening.

Closure device for sealing percutaneous opening in a vessel

Disclosed herein is a vapor therapy device for producing intra-uterine tissue effects. The device can include a shaft, including a proximal portion and a distal portion, a fluid-expandable medium, near the distal portion of the shaft, a fluid-delivery conduit, extending between the proximal portion and the distal portion of the shaft, the fluid-delivery conduit comprising an outlet, near the distal portion of the shaft, for delivery of the fluid toward the medium, and an in vivo heat generator, near the distal portion of the shaft, to heat the fluid. A method of treating a patient for menorrhagia with the device can include introducing a medium, in a contracted state, into a patient, delivering a fluid toward the medium to expand the medium in vivo; generating heat in vivo on or near the medium to vaporize the fluid, and exposing a treatment site to the vaporized fluid.

Steam ablation device for treatment of menorrhagia

A stent, shunt, or plug, for at least partial insertion into a patient, can include a deformable elongated tubular body including a proximal portion and a distal portion and defining a longitudinal lumen of the tubular body therebetween. The deformable elongated body can be capable of an expanded state and a collapsed state. The tubular body can include a sheath and a plurality of magnetizable or magnetic elements for providing magnetic repulsion, after being magnetically actuated, to maintain the tubular body to maintain the expanded state.

Magnetically deployable urinary stent

A method of treating diverticulitis while maintaining the bioactivity of the diverticulum. The devices and methods include placing an endoscopic device within a colonic lumen relative to at least one diverticulum and inserting a plurality of particles into the at least one diverticulum. The plurality of particles can include magnetic particles, non-magnetic particles, or both. The plurality of particles can partially or totally occlude the diverticulum preventing unwanted material from entering the diverticulum. Additionally, the plurality of particles can include antimicrobial and therapeutic layers that can treat diverticulitis and prevent or minimize diverticulitis from occurring.

Devices and methods to treat and prevent diverticulitis

A ureteral stent is provided. The stent may include a first section having a first wall defining a first luminal section. The stent may further include a second section having a second wall defining a second luminal section. The second section can be enabled to substantially close at times external pressure is applied to the stent.

Ureteral stent

A surgical device such as a therapy device that can allow a surgeon to treat a target tissue with ultra-violet (UV) light ablation therapy. In one example, the therapy device is configured to treat menorrhagia. In that instance, the therapy device may be configured to effect or destroy the endometrium during a procedure treating menorrhagia.

Surgical devices for treating body tissue and diagnosing patients

A modular endoscope system comprises an exoskeleton, a camera unit couplable to the exoskeleton, a therapeutic unit couplable to the exoskeleton, a steering unit couplable to the exoskeleton, and a control unit couplable to the exoskeleton. A method for building a modular endoscope comprises determining camera and therapeutic capabilities of the endoscope, selecting an exoskeleton for the endoscope, attaching a camera unit and therapeutic unit, if such capabilities are determined, to the selected exoskeleton to satisfy the determined capabilities, and attaching a control unit to the exoskeleton to control any camera unit and therapeutic unit attached to the exoskeleton. A method of processing modular endoscope components for performing a surgical procedure comprises identifying a patient to receive a treatment, selecting components of the endoscope to perform the treatment, treating the patient with the endoscope, and deconstructing the components of the endoscope into reusable and disposable components.

Insertion sheath for modular disposable endoscope components

Disclosed herein is ureteral stent. The ureteral stent includes a proximal end, a distal end, and a middle portion. The proximal end includes a retention feature having a coiled shape. The distal end is opposite the proximal end. The middle portion is between the proximal end and the distal end.

A therapy device comprises a shaft extending between proximal and distal portions, a surgical instrument located at the distal portion, a handpiece located at the proximal portion, a treatment end located at the distal end of the surgical instrument that can apply photodynamic therapy (PDT). The treatment end includes an applicator to apply a photosensitizer to a surface of a target tissue and a light emitter that can emit generated phototherapeutic light to activate the photosensitizer to ablate target tissue. A method for providing PDT to the target tissue includes inserting the therapy device into the patent, applying the photosensitizer and phototherapeutic light to a surface of the target tissue, and removing the device from the patient.

Photodynamic therapy device and methods of use

Surgical forceps can include a drive pin an outer tube, a first jaw, a second jaw, and an inner tube. The outer tube can define a longitudinal axis. The first jaw can be pivotably connected to the outer tube. The first jaw can include a pair of flanges located at a proximal portion of the first jaw, where each flange can include a track receiving the drive pin. The inner tube can be located within the outer tube and can extend along the longitudinal axis. The inner tube can include a pair of arms extending from a distal portion of the inner tube. The drive pin can be securable to the pair of arms. The inner tube can be translatable within the outer tube to drive the drive pin along the tracks to move the second jaw between open and closed positions.

Forceps drive shaft

Provided is a ureteral stent comprising certain amount of ethylene-vinyl acetate polymer and a certain amount of an additive selected from barium sulfate, bismuth subcarbonate, bismuth oxychloride, a polyolefin elastomer, a thermoplastics elastomer, and a mixture thereof. The provided stent may have multiple layers such as inner layer and outer layer with each layer having different elastic modulus. Also provided is a method of making the aforementioned ureteral stent and a method of using the ureteral stent in treating kidney or bladder related diseases.

A forceps having at least a first jaw with a longitudinal axis is disclosed. The first jaw can include a body portion, a first flange, a second flange and a cam pin. The first flange can define a first cam slot with a longitudinal extent along the longitudinal axis. The second flange can be spaced from the first flange a distance transverse to the longitudinal axis of the first jaw and can have a second cam slot. The cam pin, with a longitudinal axis, can be moveably secured within the first cam slot and the second cam slot. A diameter of the cam pin can be less than a width between a first longitudinal edge that defines a first side of each of the first cam slot and the second cam slot and a second longitudinal edge that defines a second opposing side of each of the first cam slot and the second cam slot so that the cam pin is moveably received by both the first cam slot and the second cam slot. With the first jaw pivoted to at least a first position, the cam pin and first flange can be configured such that the first longitudinal edge is contacted by the cam pin but the second longitudinal edge is spaced from the cam pin. The cam pin and second flange can be configured such that the first longitudinal edge is spaced from the cam pin but the second longitudinal edge is contacted by the cam pin.

Forceps with intentionally misaligned pin

Surgical instruments and methods are disclosed including a tissue removal tool for treatment of endometrial tissue on a background tissue of a patient. The tissue removal tool can optionally comprise a graspable portion, a shaft and an end effector. The shaft can be coupled to the graspable portion. The shaft can have a proximal portion and a distal portion and can be configured to access an anatomic location of the endometrial tissue. The end effector can be coupled to the distal portion of the shaft. The end effector can be configured to lift the endometrial tissue relative to the background tissue to a lifted position. The end effector can be configured to cut the endometrial tissue from the background tissue with the endometrial tissue in the lifted position.

Surgical device for treatment of endometriosis

An endoscope can comprise a proximal section, an insertion section extending longitudinally from the proximal section and comprising an elongate tubular body disposed along an insertion section longitudinal axis and a lumen extending through the elongate tubular body, and a distal section extending from the insertion section and comprising an elevator portion comprising an elevator configured to position and orient one or more endotherapy tools extending from the lumen, and a camera module comprising an illumination unit and an imaging unit. The camera module can be positioned longitudinally spaced apart from the elevator portion in an in-line configuration, such that the insertion tube longitudinal axis passes through the elevator portion and the camera module. The camera module can be user-detachable from the elevator portion. The camera module can be cleaned and sanitized for reuse and the insertion section can be disposable.

Endoscope with low-profile distal section

A ureteral stent that includes a tubular member and a retaining end adapted to be placed inside a kidney or a bladder of a patient. The retaining end includes a plurality of loops. Each of the loops are centered about a loop axis, and two or more of the loop axes extend in different directions relative to other loop axes.

Growing community of inventors

Princeton, MN, United States of America

Thomas J Holman