Abstract: A balloon fold design for efficient expansion of a side branch assembly in a bifurcated stent. The design involves forming a cup arrangement by folding the radial end of the side branch balloon structure into the luminal end of the side branch balloon structure and then folding the cup down into an orderly discus arrangement. The folding pattern allows for the side branch balloon structure to inflate in a sweeping rotational manner efficiently pushing the side branch assembly petals out and away from the main body of the stent with a low risk of the balloon becoming entangled or damaged by its contact with the petals. The design also allows for the expansion force to be applied at the appropriate time in the optimally needed direction by initially being oriented in a predominantly circumferential direction which is gradually shifting to a predominantly radial direction. In addition, the fold design reduces the overall volume and profile of the side branch balloon structure.

Abstract: In a method of ablating a tunica of a patient, a laser fiber is inserted into the tunica of the patient. Portions of the tunica are exposed to laser light discharged from the laser fiber. The portions of the tunica that are exposed to the laser light are ablated. In one embodiment, a device is used to control the exposure of the tunica to the laser light. In one embodiment, a penile prosthesis is implanted in the ablated tunica.

Abstract: Devices, methods and kits which, when installed or used, access, aspire, dilate, insufflate, drain or deliver fluid medicaments to, or place a patency device within a sinus area, such as a maxillary sinus or a maxillary sinus ostium. The device can include a hollow catheter and probe, and can be configured to permit gradual and incremental probe extension. The device can be constructed to enhance the precision and maneuverability within the nasal and sinus passageways, while also accommodating the natural anatomical geometry of a targeted paranasal treatment site. For example, the present treatment and placement device can accomplish access to the maxillary sinus ostium by utilizing an uncinate process to guide a probe tip into the ostium in a retrograde manner. The probe can be slidably, bi-directionally or co-axially positioned within the catheter. A distal portion of the probe can be biased away from a longitudinal axis of the catheter.

Abstract: The invention described herein provides for a simple, economical system and method for reducing environmental release of dental amalgamous mercury from teeth caused by cremation of corpses. The invention controls and reduces the amount of mercury released using a pre-crematorial and non-disfiguring system and method. The system of the invention can include a dental containment and applicator delivery system to apply a curable thermal protectant composition onto the teeth. The composition coating significantly inhibits the extent of thermal destruction of the tooth per se including its amalgam filling content.

Abstract: The invention provides an embolic filter, a support structure therefor, and methods for preparing said filter for deployment and retrieval.

Abstract: According to an aspect of the present invention, medical devices are provided which comprise a metallic region and a coating on all or part of the metallic region that comprises a multivalent acid.

Abstract: A crimping fixture for crimping a stent onto a balloon of a catheter is disclosed. The crimping fixture includes a flexible elastomeric body having a crimping lumen and one or more inflation lumens extending through the flexible elastomeric body. The flexible elastomeric body is elastically stretched such that a pre-crimped stent may be placed in the crimping lumen. The inflation lumens are then pressurized with a fluid to impart an inward crimping force onto the stent to crimp the stent to a balloon.

Abstract: A device includes a sheath having a lumen defined by a wall. The wall has an outer surface that is configured to emit ultraviolet light in a direction substantially normal to the wall. The lumen has a distal end configured for percutaneous placement. The lumen has a proximal end configured to receive a catheter.

Abstract: In a method of ablating a tunica of a patient, a laser fiber is inserted into the tunica of the patient. Portions of the tunica are exposed to laser light discharged from the laser fiber. The portions of the tunica that are exposed to the laser light are ablated. In one embodiment, a device is used to control the exposure of the tunica to the laser light. In one embodiment, a penile prosthesis is implanted in the ablated tunica.

Abstract: A stent formed from a bioabsorbable polymer matrix including at least one bioabsorbable polymer and at least one therapeutic agent dispersed therein, and methods of making the same.

Abstract: A balloon folding device comprises a first die having an external contacting surface and a second die having a cavity. A portion of the cavity comprises a contacting surface shaped complimentary to the external contacting surface of the first die. The second die is movable with respect to the first die. A balloon catheter having a primary balloon and a secondary balloon is oriented with the secondary balloon located between the first die and the second die. The secondary balloon is folded by moving the second die toward the first die until the contacting surfaces of the dies contact, fold and deflate the secondary balloon. In some embodiments, the dies are moved until at least a portion of the external contacting surface of the first die is oriented within the cavity of the second die.

Abstract: A medical device for capturing emboli from a blood vessel. An example medical device may include an elongated guide member. The elongated guide member may include a proximal end, a distal end, a first conductive lead, and a second conductive lead. The medical device may also include a power source connected to the first conductive lead and the second conductive lead. The medical device may also have a filter having a proximal end and a distal end, wherein the proximal end is coupled to the first and second conductive leads. The activation of the power source may transition the filter from a first compressed shape to a second expanded shape.

Abstract: The disclosure describes an embolic filter and a support structure therefor.

Abstract: A balloon folding system specifically configured to reduce a side branch balloon of a bifurcated balloon catheter assembly includes a die that defines at least one chamber for receipt of the sidebranch balloon, and at least one pin sized to fit into the chamber and reduce the balloon to a substantially flattened state. The system also may include a housing for the reduction and folding of a primary branch balloon. The system is configurable to fold and reduce both branches simultaneously or separately.

Abstract: The invention provides an embolic filter, a support structure therefor, and methods for preparing said filter for deployment and retrieval.

Abstract: An intravascular distal protection device, comprising a guidewire having a proximal end and a distal end, a filtering material disposed about the guidewire, the filtering material having a proximal edge defining a proximally facing opening when in an expanded position, a hoop wire having a proximal end and a distal end and slidably attached to the proximal edge, the hoop wire wrapped in a helical coil about the guidewire in a first contracted position and defining a hoop at the proximal end of the filtering material in the expanded position, and an actuation member attached to the hoop wire and extending at least substantially to the proximal end of the guidewire and configured to move the hoop wire between the first contracted position and the expanded position.

Abstract: A balloon folding device comprises a first die having an external contacting surface and a second die having a cavity. A portion of the cavity comprises a contacting surface shaped complimentary to the external contacting surface of the first die. The second die is movable with respect to the first die. A balloon catheter having a primary balloon and a secondary balloon is oriented with the secondary balloon located between the first die and the second die. The secondary balloon is folded by moving the second die toward the first die until the contacting surfaces of the dies contact, fold and deflate the secondary balloon. In some embodiments, the dies are moved until at least a portion of the external contacting surface of the first die is oriented within the cavity of the second die.

Abstract: Devices, methods and kits which, when installed or used, access, aspire, dilate, insufflate, drain or deliver fluid medicaments to, or place a patency device within a sinus area, such as a maxillary sinus or a maxillary sinus ostium. The device can include a hollow catheter and probe, and can be configured to permit gradual and incremental probe extension. The device can be constructed to enhance the precision and maneuverability within the nasal and sinus passageways, while also accommodating the natural anatomical geometry of a targeted paranasal treatment site. For example, the present treatment and placement device can accomplish access to the maxillary sinus ostium by utilizing an uncinate process to guide a probe tip into the ostium in a retrograde manner. The probe can be slidably, bi-directionally or co-axially positioned within the catheter. A distal portion of the probe can be biased away from a longitudinal axis of the catheter.

Abstract: Devices, methods and kits which, when installed or used, urge or maintain patency of sinus ostia, such as the ostium between a nasal passageway and a maxillary sinus, while maintaining some function of cilia extending within or near the ostium. In various examples, the devices comprise a first portion, a second medial portion including a partially open cross-sectional configuration, and a third portion including one or more flexible and outwardly-biased projections. The partially open cross-sectional configuration can maintain a track of uncovered cilia within and near the ostium. In some examples, the devices can include an asymmetric body configuration. In some examples, the first portion includes a U-shaped configuration and the third portion includes at least two flexible and outwardly-biased projections. In some examples, the first, second or third portion includes a medication for delivery into sinus tissues.

Abstract: The invention is directed to mechanisms and methods that reduce the delamination of a therapeutic agent from a stent. The mechanisms include holes (channels, wells, and other hole configurations), protrusions, sintered metal cores, clamps/staples, pins, and stainless steel shields.