Medtronic, Inc.

Coloplast A/s

Yelena G Tropsha

John Matthew Swoyer

Eric H Bonde

Mark A Christopherson

Julie M Woessner

Geoffrey A Daniel

Kevin M Cristadoro

Warren L Starkebaum

Carole A Tronnes

Eric M Stetz

Thomas Chun

Chris A Deegan

An indicator element of a percutaneous needle guide for a medical scanning device includes a pointer for pointing to a percutaneous needle entry site on an epidermis of a body, when the guide is attached to the device and the device is positioned over the epidermis for scanning. A user may orient and insert a needle into the entry site according to the direction of the pointer, by just viewing the pointer, without the needle being constrained by the pointer. The guide may include an adjustment mechanism for moving the indicator element with respect to the device, when the guide is attached to the device; the adjustment mechanism moves the indicator element, without changing an orientation of the pointer, in a direction approximately parallel to a plane that is approximately tangent with an apex of the device transducer surface and approximately perpendicular to a longitudinal axis of the device.

Percutaneous needle guide and methods of use

A method of implanting a penile prosthetic in a patient includes providing an implantable cylinder with a resorbable component attached to an exterior surface of the implantable cylinder and a tow line engaged with the resorbable component. The method includes inserting the tow line into a corpora cavernosum of a penis, directing the tow line through a glans of the penis, and pulling on the tow line and moving the implantable cylinder into the corpora cavernosum of the penis. The method includes locating a distal end of the implantable cylinder in a distal location in the corpora cavernosum of the penis, and disengaging the tow line from the resorbable component.

Method of implanting a penile prosthetic in a patient

A method of implanting a penile prosthetic includes confirming that a tow suture is coupled with a resorbable suture-engagement component attached to an exterior surface of a cylinder. The method includes inserting the tow suture into a corpora cavernosum of a penis and pushing the tow suture through a glans of the penis and pulling on the tow suture and towing the cylinder to a distal location within the penis. The tow suture is removed from the resorbable suture-engagement component.

Method of implanting a penile prosthetic

Disclosed is a penile prosthetic including a cylinder and a resorbable suture-engaging component attached to an exterior surface of the cylinder. The suture-engaging component is attachable to a suture to allow a surgeon to pull the cylinder in a distal direction into the penis. During the healing time after the surgery, the resorbable suture-engaging component is resorbed into the tissue of the penis.

Resorbable suture-engagement component for a penile prosthetic

Methods and apparatus for ablating a target tissue are discussed. Such methods and apparatus include those that simplify tissue ablation. For example, a tissue ablation device having an actuator, such as a trigger mechanism, coupled to a power source and an electrode is discussed. A single step of engaging the actuator causes the electrode to be introduced into the target tissue and causes energy to be delivered from the power supply to the tissue via the electrode. Devices that include an electrode actuator for causing the electrode to be introduced into the target tissue and a fluid actuator for causing the fluid to flow to the target tissue are also discussed. Methods of causing the electrode to be introduced into the target tissue and fluid to flow to the target tissue with a single step and more than one step are also discussed.

Tuna device with integrated saline reservoir

Methods and apparatus for ablating a target tissue are discussed. Such methods and apparatus include those that simplify tissue ablation. For example, a tissue ablation device having an actuator, such as a trigger mechanism, coupled to a power source and an electrode is discussed. A single step of engaging the actuator causes the electrode to be introduced into the target tissue and causes energy to be delivered from the power supply to the tissue via the electrode. By way of additional example, a tissue ablation device having an actuator coupled to a fluid source and an electrode is discussed. A single step of engaging the actuator causes conductive fluid to flow from the fluid source to the target tissue location and causes the electrode to be introduced to the target tissue location. The fluid source may be a conductive fluid, such as saline, which may increase the efficiency of ablation. Various other configurations and methods that simplify tissue ablation are also discussed.

A locating guide for locating a target tissue site within a patient includes a body, a first substantially radiopaque reference marker on the body, and a second substantially radiopaque reference marker extending from a major surface of the body. The reference markers provide reference points that extend in at least two dimensions, and may be useful for registering a medical image of tissue with an actual location on or within the patient in order to more accurately and precisely locate a target tissue site within the patient. In some embodiments, the second reference marker is oriented at a predetermined angle relative to the major surface of the body, and provides a guide that a clinician may reference in order to orient a medical element introducer when introducing the introducer into the patient to access a particular target tissue site.

Locating guide

A bulking device for implantation into a lumen wall that includes a bulking material that is configured to alter the portion of the lumen into which it is implanted and one or more therapeutic substances in association with the bulking material, wherein the device is configured to alter the portion of the lumen wall into which it is implanted. A method for inserting devices of the invention are also included.

Devices for augmentation of lumen walls

Percutaneous needle guide

TUNA device with integrated saline reservoir

One or more tissue bulking devices are implanted to bulk a structure within a patient. The tissue bulking devices may be implanted between the structure and an adventitial layer that at least partially covers the structure, or within the adventitial layer. In some embodiments, the structure is a luminal wall that defines an inner lumen, and the bulking devices are implanted endoscopically via the lumen. In such embodiments, the tissue bulking devices may be implanted between a muscular layer of the luminal wall and an adventitial layer that at least partially covers the luminal wall, or within the adventitial layer. In exemplary embodiments, the luminal wall is the wall of the esophagus of the patient, and the tissue bulking devices are implanted proximate to the lower esophageal sphincter (LES) of the patient to treat gastroesophageal reflux disease (GERD).

Implantation of tissue bulking devices

Delivery elements, including needle electrodes and sheaths of tissue ablation devices, containing a conductivity-enhancing agent are discussed. The delivery elements contain a body member and optionally one or more coating layers. The conductivity-enhancing agent is disposed on or in the body member and/or at least one of the one or more coating layers. The conductivity-enhancing agent is capable of eluting from the delivery element when the delivery element is contacted with bodily tissue or fluid and increases conductivity of the tissue, making tissue ablation more efficient.

Growing community of inventors

Plymouth, MN, United States of America

Yelena G Tropsha