Abstract: A depth camera illuminator with a superluminescent light-emitting diode (SLED) in a motion tracking system. One or more SLEDs have a sufficient power, such as 75-200 milliwatts, to extend in a field of view in an area such as a room in a home. To correct for chromatic aberration which would otherwise exist due to the wider range of wavelengths which are emitted by an SLED compared to a laser, an achromatic diffractive optical element is used to disperse the light over the field of view. The achromatic diffractive optical element can have a stepped multi-level profile with three or more levels, or a continuous profile. Based on a tracked movement of a human target, an input is provided to an application in a motion tracking system, and the application performs a corresponding action such as updating a position of an on-screen avatar.

Abstract: An applicator device for use in surgical procedures is disclosed. The device includes an applicator assembly, an atomizing tip, and a regulator assembly. The applicator assembly has a handle, an applicator intake port and a double-barreled syringe. The double-barreled syringe includes a first cylinder and a second cylinder. The atomizing tip is provided at a distal end of the handle and the atomizing tip is in fluid communication with the double-barreled syringe. The atomizing tip includes a proximal end configured to receive and mix a first and a second composition from the double-barreled syringe. The regulator assembly includes a first regulator, a second regulator and a third regulator. The first regulator is configured for engagement with the first cylinder, the second regulator is configured for engagement with the second cylinder, and the third regulator is configured for engagement with the applicator intake port.

Abstract: The apparatus for deployment of an intravascular therapeutic device, includes an elongated, flexible pusher member and a therapeutic device connected to a severable portion of a first connector member mounted to the flexible pusher member with an elongated second connector member connected to the therapeutic device. The first connector member or second connector member may be capable of being broken by heat, and a heat source is provided for heating and breaking the first connector member or the second connector member to release the therapeutic device.

Abstract: A transdermal permeant delivery system for delivery of at least one permeant composition into a tissue membrane of a subject including a disposable substrate having at least a portion of a bottom surface of a first release liner connected to an upper surface of the substrate and a patch having a backing layer and a reservoir that is selectively removable from the top surface of the first release liner. In a connected position, a first portion of the backing layer of the patch is releaseably mounted to a top surface of the first release liner in spaced registration with a poration area of the substrate.

Abstract: An elongate medical device having an axis comprises an inner liner, a jacket radially outward of the liner, a braid comprising metal embedded in the jacket, a sensor, and at least one wire electrically connected to said sensor. The at least one wire is one of: embedded in the jacket and optionally disposed helically around the braid; extending longitudinally within a tube which extends generally parallel to the device axis and wherein the tube is embedded in the jacket; and disposed within a lumen, wherein the lumen extends longitudinally within the jacket.

Abstract: A safety pen needle assembly is provided herein which includes a hub and a needle fixed to the hub. Further, a first shield is provided, along with a second shield which has a biasing element disposed to urge the second shield proximally towards a proximal end of the needle. The assembly further includes a releasable retaining assembly for releasably retaining the second shield in an initial position against the force of the biasing element. A predetermined extent of movement of the first shield causes the retaining assembly to release the second shield, and, wherein, with the second shield being released, the second shield is urged proximally by the biasing element to a second position where the second shield covers the proximal end of the needle. Advantageously, with the subject invention, an assembly is provided which allows for passive activation of a shield on a non-patient end of a pen needle assembly by a patient-end shield.

Abstract: An insufflation gas warmer and humidifier apparatus and methods are provided. Insufflation gas is received from a bulky insufflation tubing. Insufflation gas received travels through, in one aspect, a channel or winding flow path, in a passage. The configuration of the passage ensures that the insufflation gas, which travels through the passage, receives sufficient heat and moisture. A humidifying reservoir humidifies the insufflation gas as the insufflation gas is passed to the passage. In one aspect, an oxygenator introduces slight amounts of oxygen into the insufflation gas. A warmer connected to the passage warms the gas in the passage. The warmer, in one aspect, contains a reactive agent that when exposed to air produces heat that is transferred to the passage to warm the insufflation gas within the passage.

Abstract: An insertion device and insertion set. The insertion device for inserting at least a portion of at least one piercing member of an insertion set through the skin of a patient includes a device housing, a carrier body and a driver. The carrier body is slidably received within the device housing for movement between an advanced position and a retracted position. The carrier body also includes a receiving structure to support the insertion set in a position with the at least one piercing member oriented for insertion through the skin of the patient at a predetermined angle relative to the skin of the patient upon movement of the carrier body from the retracted position to the advanced position.

Abstract: An implantable port includes a body with a reservoir in the body, a tunnel extending from the reservoir to an outer surface of the body, a pivoting coupling connected to the body near the tunnel on the outer surface, and a stem connected to the pivoting coupling.

Abstract: The invention concerns a medical tubing assembly (100) comprising: finned medical tubing (10) formed from an elongate tubular member (20) disposed with one or more longitudinal fins (21, 21?, 21?), a collar (200), slidably mountable on the finned tubing (10), equipped with a locking means and optionally one or more suture eyelets (250, 250?), said locking means configured to provide a locking force against one or more of the longitudinal fins (21, 21?, 21?). The invention allows securing of a medical tubing in situ that prevents slippage or damage to the tubing wall.

Abstract: A connector and method of connecting are described for connecting a first and second catheter at an overlap area where the first catheter fits within the second catheter. The connector includes a collar that surrounds a portion of the overlap area and a clamp that applies a radially inward force to the collar and encircles a portion of the overlap area.

Abstract: A connector and method of connecting are described for connecting a first and second catheter at an overlap area where the first catheter fits within the second catheter. The connector includes a collar that surrounds a portion of the overlap area and a clamp that applies a radially inward force to the collar and encircles a portion of the overlap area.

Abstract: An image processing system includes an object illuminated by a pre-determined first spectrum of light and an array of fringe lines, an imaging device configured to capture an image of the object including the first spectrum of light and the fringe lines reflecting from a surface of the object, and a processor in signal communication with the imaging device to receive an input data representing the image of the object, wherein the processor: generates a first data model based on the input data; removes a DC-component from the first data model to create a second data model; and performs a two dimensional Fourier transform profilometry based on the second data model.

Abstract: A guidewire includes a core shaft and a coil body wound around an outer periphery of the core shaft. A distal end portion of the core shaft and a distal end portion of the coil body is fixed to each other to form a most distal end portion. The coil body includes a linear portion and a bent portion, the linear portion extending in a distal direction from a proximal end of the coil body, the bent portion being provided on a distal side of the liner portion. The core shaft and the coil body located in the bent portion are fixed to each other with a fixing member.

Abstract: An electrosurgical tool can be used to fuse tissue. The electrosurgical tool can include a jaw assembly, an elongate shaft, and a handle assembly. Actuation of the handle assembly can actuate the jaw assembly. The elongate shaft can be rotatable without disrupting electrical connection to the jaw assembly. The electrosurgical tool can include a cutting blade to separate fused tissue. The electrosurgical tool can also include a jaw assembly configuration or an exterior cutting electrode to improve surgical access with the tool.

Abstract: Color correction of an autostereoscopic color display capable of displaying multiple views of one scene. Multiple viewing regions of the autostereoscopic color display are identified. The multiple viewing regions together comprise the whole of an operating viewing zone for the autostereoscopic color display. A respective plurality of color correction LUTs are constructed. At least one color correction LUT is constructed for each different viewing region. Color correction LUTs corresponding to current viewing regions are selected based on information regarding viewer location. The selected color correction LUTs are applied to the autostereoscopic color display.

Abstract: An electrosurgical system can include an electrosurgical generator, a feedback circuit or controller, and an electrosurgical tool. The feedback circuit can provide an electrosurgery endpoint by determining the phase end point of a tissue to be treated. The electrosurgical system can include more than one electrosurgical tool for different electrosurgical operations and can include a variety of user interface features and audio/visual performance indicators. The electrosurgical system can also power conventional bipolar electrosurgical tools and direct current surgical appliances.

Abstract: Phase end point determination is provided to automatically halt the application of energy to tissue. Prior to the application of energy, the phase end point determination is identified by measuring the product of permittivity and conductivity of the tissue to be treated.

Abstract: A medical treatment administration system for delivering a medical treatment to a patient. The system has a medical device, an electronic processor coupled to the medical device, and a sensor coupled to the processor. The sensor receives one or more signals which it transfers to the processor. The signals can be derived from the patient's physiological condition and/or the environment of the patient. The processor receives the signals and performs a calculation of the signal. Based on the result of the calculation, the processor regulates the distribution of medical treatment to the patient over a period of time.

Abstract: Systems and methods for delivering drugs or other substances to target locations outside of blood vessel lumens or other body lumens. In some embodiments, a catheter having a penetrator is advanced into the body lumen and the penetrator is then advanced from the catheter toward a target location outside of that body lumen. The substance is then delivered through a the penetrator itself or through a delivery catheter that has been advanced through the penetrator to the target location. In other embodiments, the blood vessel or other body lumen is blocked at spaced-apart first and second locations and a quantity of the substance is introduced into the closed-off body lumen between the blocked first and second locations. The substance then diffuses into or through the wall of the vessel or body conduit to reach the target location.