Abstract: A sensor cartridge comprising a sterile capsule. The sensor cartridge further comprises a sensor within the sterile capsule. The sensor cartridge further comprises a sensor connector connected to the sensor in an initial position. The sensor cartridge further comprises an insertion needle for inserting the sensor into a subject. The insertion needle is within the sterile capsule. The sensor cartridge further comprises a sensor mounting unit for receiving the sensor connector at a mounted position. The sensor mounting unit comprises an adhesive surface for attaching to an exterior surface of the subject. The sensor cartridge further comprises an insertion mechanism operable for actuating the insertion needle and moving the sensor connector from the initial position to the mounted position.

Abstract: The invention concerns the domains of materials science and medicine and relates to a method such as can be applied to in vivo or in vitro fertilization, for instance. The problem addressed by the present invention is that of specifying a method with which the activity and controlled mobility of motile cells is improved and the absorption of materials alien to the cell is prevented as far as possible. The problem is solved by a method in which one or more motile cells are introduced into or attached to one or a plurality of magnetic particles, and subsequently the magnetic particles with the motile cells introduced into them or attached to them are moved in a directional manner by the application of an external magnetic field. The problem is further solved by the use of the method for the controlled movement of motile cells in liquid or gaseous media in the body of a mammal or human being.

Abstract: A clamping device for attaching to an external fixation element of an external fixation system includes a first jaw having an inner surface and an outer surface and includes a second jaw having an inner surface and an outer surface, with the inner surface of the first jaw and the inner surface of the second jaw together forming a passage configured to receive the external fixation element of the external fixation system. A locking system is engageable with the first and the second jaws and is moveable relative to the first and the second jaws between at least a first position.

Abstract: A spinal stabilization system having a pedicle screw which includes (i) a shaft with external threads and a head segment on one end of the shaft; (ii) a first drive socket positioned in the head segment; (iii) a second drive socket on a shaft end opposite the first drive socket; and (iv) wherein the shaft end opposite the first drive socket has a lesser diameter than the shaft end at the head segment. The system further includes an intervertebral stabilization structure having an elongated body with rotating ring segments attached to each end of the elongated body.

Abstract: A polyaxial bone screw assembly includes a threaded shank body having an integral upper portion receivable in an integral receiver, the receiver having an upper channel for receiving a longitudinal connecting member and a lower cavity cooperating with a lower opening. A down-loadable compression insert, a down-loadable friction fit split retaining ring having inner and outer tangs and an up-loadable shank upper portion cooperate to provide for pop- or snap-on assembly of the shank with the receiver either prior to or after implantation of the shank into a vertebra. The shank and receiver once assembled cannot be disassembled.

Abstract: Anterior cervical instrumentation systems, methods, and devices are disclosed. Systems may facilitate immobilizing or providing support for the cervical portion of the vertebral column of a patient. A device may comprise a plate having two channels located in a proximal to distal direction, and may further comprise at least one aperture. The device may further comprise attachment elements such as attachment cross-links and spacer cross-links, and fasteners. The plate and the attachment elements may be secured to the vertebrae by passing fasteners through apertures and channels. The length of the plate, position and number of the attachment cross-links, position and number of spacer cross-links and degree of movement may be intraoperatively selected by the surgeon to provide an optimal application and procedural outcome. Uniform components of the devices and systems allow for a more streamlined and simplified method of treating spinal conditions.

Abstract: Various embodiments described herein provide interspinous process spacing devices and related systems and methods. In one embodiment, surgical instrument system for implanting an interspinous process spacing device includes a first arm having a proximal end, an elongated central portion, and a distal end, wherein the distal end includes a first engagement element configured for releasably engaging a first attachment side of an interspinous process spacing device. The system also includes a second arm having a proximal end, an elongated central portion, and a distal end, wherein the distal end includes a second engagement element configured for releasably engaging a second attachment side of the interspinous process spacing device. The first arm and the second arm are removably attachable to one another via attachment elements and are configured for aligning a spacer of the first attachment side and a spacer opening of the second attachment side.

Abstract: A device for treating fractures, comprises an intramedullary member sized and shaped for insertion along a longitudinal axis of a bone within a medullary canal thereof, the intramedullary member including an opening extending obliquely therethrough, the opening, when the intramedullary member is in a desired position within a bone, aligning with a desired axis along which an implant is to be inserted into a bone, the intramedullary member including a channel formed therewithin and opening to the opening and a locking mechanism mounted in the channel, the locking mechanism including a locking abutting structure extending into the opening in combination with an implant sized to be slidably received through the opening and inserted along the desired axis, the implant including a plurality of implant abutting structures aligned to engage the locking abutting structure preventing medial movement of the implant relative to the intramedullary member.

Abstract: The present invention relates to a jawbone distraction system and control method thereof, including a jawbone extension apparatus, a remote controller and a monitor, the jawbone distractor being configured to allow a horizontal shift of alveolar bone as well as performing vertical jawbone distraction, being precisely controlled in a wireless mode and configured to control a drive of the jawbone distractor through the remote controller while ascertaining a driving state by the monitor.

Abstract: An orthopedic bone plate constructed from shape memory material provides the ability to move from an open shape to a compressed shape and create compression on two bones or bone fragments to encourage healing. The plate may be any umber of shapes, with two or more screws anchoring the plate to bone. The plate is affixed to bone in a sequence of steps that involve first placing the plate on an insertion tool, attaching drill guide tubes, placing the plate over bone, drilling holes in bone, and then attaching the plate to the bone via screws. The insertion tool can then be removed at the surgeon's convenience allowing compression on the two bones.

Abstract: A pedicle screw may include an electrically conductive portion formed from a material having a greater electrical conductivity than that of the base material from which the screw is formed. The electrically conductive portion preferentially channels electrical energy supplied by an electrical probe to a location of the electrically conductive portion facing the nerve root. The portion thus provides a sort of electrical highway that helps to focus the electrical energy applied to the pedicle screw in a particular direction, towards the presumed location of the nerve root. As an alternative to placement of the electrically conductive portion in the pedicle screw itself, the electrically conductive portion could be placed within a tap that is used in preparing the pedicle for receipt of the pedicle screw (e.g., in forming the threaded structure in the pedicle bone into which the pedicle screw will then be placed).

Abstract: The present disclosure relates to a device for use during ligament reconstruction surgery. The device includes a handle and a shaft coupled to the handle, the handle including a first channel for housing of an insert, a second channel, a third channel for housing of the shaft, a first window, a second window, and a groove. A method for use during ligament reconstruction surgery is also disclosed.

Abstract: A method of operating a medical system, including coupling a medical system to an outlet of a fluid distribution network having a plurality of fluid outlets in a patient treatment center; delivering fluid from the outlet to the medical system; compressing the delivered fluid with the medical system; decreasing the moisture content of the delivered fluid with the medical system; cooling the fluid with the medical system; delivering the fluid from the medical system to a medical device; and removing the fluid from medical device with the medical system.

Abstract: Systems, methods, and other embodiments associated with characterizing Radio Frequency Ablation (RFA) lesions using Optical Coherence Tomography (OCT) are described. One example method includes acquiring an OCT signal from a Region Of Interest (ROI) in an ablated material. The example method may also include determining whether a lesion was formed by the ablation by analyzing optical properties of the ROI as recorded in the OCT signal.

Abstract: A surgical device having a step-up converter, a power supply unit and a control arrangement. The step-up converter converts a mains AC voltage to an intermediate circuit voltage and energizes a DC intermediate circuit. The power supply unit includes an inverter connected to the intermediate circuit. The power supply unit also includes a transformer that has a primary coil connected to the inverter and a secondary coil for energizing a load. The control arrangement includes a PFC control circuit connected in a controlling manner to the step-up converter. The control arrangement further includes an operation control circuit connected in a controlling manner to the power supply unit. The PFC control circuit and operation control circuit are connected to each other via a digital communication interface.

Abstract: Systems and methods for analyzing an electrosurgical unit are provided. One system includes an electrosurgical unit analyzer having an input configured to receive radio frequency (RF) signals from an electrosurgical generator and a measurement subsystem configured for programmable waveform detection corresponding to the received RF signals. The measurement subsystem includes a field-programmable gate array (FPGA) defining one or more thresholds for the waveform detection. The electrosurgical unit analyzer further includes a user interface displaying information relating to individual pulses detected from the RF signals.

Abstract: A method and system for treating a surgical incision to prevent scarring is disclosed. The system comprising an applicator is configured to protrude a target tissue from one or both sides of a surgical incision into a treatment cavity located in the applicator. The system is further configured to deliver fractional treatment, from energy sources located along the inner walls of the treatment cavity, to an incision edge.

Abstract: An electrosurgical probe for suction and irrigation systems is provided. The electrosurgical probe comprises an elongate tube with a probe tip and a probe handle. An unobstructed fluid communication path is defined by the probe handle and elongate tube.

Abstract: Regions of tissue having reduced electrical propagation are created in a bladder to affect its electrical or mechanical properties. To create these tissue regions, a tubular device is advanced through the urethra leading to the interior of the bladder, a distal expandable structure of the device is expanded to contact the inner wall of the bladder, and electrodes or other active energy delivery elements of the device are activated to deliver ablation energy. The electrodes or other active energy delivery elements are disposed over the expandable structure which is shaped to conform to the interior of the bladder. The inner wall of the organ is ablated in a predetermined pattern. The same or other electrodes disposed over the expandable structure can used to electrically map the bladder. This map of electrical activity can be used to create the predetermined pattern.

Abstract: Methods, systems and devices for evaluating the integrity of a uterine cavity. A method comprises introducing transcervically a probe into a patient's uterine cavity, providing a flow of a fluid (e.g., CO2) through the probe into the uterine cavity and monitoring the rate of the flow to characterize the uterine cavity as perforated or non-perforated based on a change in the flow rate.

Abstract: Medical devices are described for performing mapping, ablating, and/or pacing procedures on one or more layers of the cardiac wall via an epicardial approach in a minimally invasive (e.g., orthoscopic) surgical procedure. One of the medical devices described includes a main support member and one or more secondary support members extending outwardly from the main support member having electrodes configured to receive electrical impulses. The secondary support member may include a support pad configured to be removably attached to a corresponding area of the epicardium for holding the medical device in place during a procedure, such as through application of vacuum pressure via a containment dome provided on each secondary support member. Further, an ablating electrode may be slidably disposed along the main support member for transmitting energy to a target site proximate the electrode. Associated methods are also described.

Abstract: Methods for treating hyperaldosteronism with therapeutic renal neuromodulation and associated systems and methods are disclosed herein. One aspect of the present technology, for example, is directed to methods that at least partially inhibit sympathetic neural activity in renal nerves proximate a renal blood vessel of a human patient. One or more measurable physiological parameters corresponding to hyperaldosteronism of the patient can thereby be improved. Moreover, central sympathetic drive in the patient can be reduced in a manner that treats the patient for hyperaldosteronism. Renal sympathetic nerve activity can be modulated along the afferent and/or efferent pathway. The modulation can be achieved, for example, using an intravascularly positioned catheter carrying a neuromodulation assembly, e.g., a neuromodulation assembly configured to use electrically-induced, thermally-induced, and/or chemically-induced approaches to modulate the renal nerve.

Abstract: A device for manipulating a magnetic coupling force across tissue in response to a monitored coupling force is described. The device includes a magnetic field source assembly, a positioning assembly operatively connected to the magnetic field force assembly, and a magnetic coupling force monitor. The magnetic field source assembly includes magnets that provide an external magnetic field source for providing a magnetic field across tissue. The positioning assembly adjusts the position of the magnetic field source. The magnetic field creates a magnetic coupling force between the external magnetic field source and an object positioned in use in a patient during a procedure, wherein the object has or is associated with an internal magnetic field.

Abstract: The various embodiments disclosed herein relate to modular medical devices, including various devices with detachable modular components and various devices with pivotally attached modular components. Additional embodiments relate to procedures in which various of the devices are used cooperatively. Certain embodiments of the medical devices are robotic in vivo devices.

Abstract: A suspension system for supporting surgical devices inside a patient's body cavity comprising an external frame, a plurality of elongated members extending from the external frame and through the patient's skin into the body cavity, and an internal platform located inside the body cavity. The internal platform includes a plurality of links reconfigurable from a first elongated position wherein the links are substantially aligned along a longitudinal axis for insertion to a second position wherein the links are angled with respect to one another to form a non-linear configuration. A first support of the external frame is movable with respect to the second support to thereby move the internal platform.

Abstract: An apparatus comprises a robotic manipulator and a surgical instrument mounted to the robotic manipulator. The surgical instrument comprises an elongate arm including an actively controlled bendable region including at least one joint region and an end effector and a passively bendable region including a distal end coupled to the actively controlled bendable region. An actuation mechanism extends through the passively bendable region and is coupled to the at least one joint region to control the actively controlled bendable region. A channel extends through the elongate arm, and an optical fiber is positioned in the channel. The optical fiber includes an optical fiber bend sensor in at least one of the passively bendable region or the actively controlled bendable region.

Abstract: A system includes a medical instrument that includes a termination fixture, an actuated element, and drive members coupled to the actuated element and extending to the termination fixture. The termination fixture provides an interface that exposes portions of the drive member to direct movement by an external system that may include a manipulator and a sterile barrier.

Abstract: A surgical sponge counter includes a unitary molded plastic sponge tray defining a plurality of wells each sized to hold a lap sponge. Each well has a ledge defining a recess below the sponge for collecting fluid once the sponge is replaced in the tray. A needle counting receptacle tray may be nested within the sponge tray above the sponges.

Abstract: Disclosed is a skin dilator, comprising an expander (11), a pipe network provided on the skin-side surface wall (111) of the expander (11) composed of longitudinal tube (22) and horizontal tube (21) having a reticular structure and communicating with each other, and a guide tube (24) communicating with the pipe network. The skin dilator further comprises several burrs (25) distributed on the skin-side surface wall (111) of the expander (11), and several small apertures (23) communicating the inner cavity of the tube with the outside are provided on both of the longitudinal tube (22) and horizontal tube(21). The tissue expander can be infused biological agents by the filling port to the skin expanding site through the small apertures (23), which may accelerate the expansion growth of skin, prevent skin complications, such as necrosis.

Abstract: While detecting a cardiac arrhythmia, a mapping electrode of a probe is used to associate a local activation time with a first location in a region of interest in the heart. While detecting an absence of the cardiac arrhythmia, the local activation time is associated with a second location in the heart. Electrical data of the first location is assigned to the second location, and an electroanatomic map of the heart is generated that includes the second location in association with the assigned electrical data of the first location.

Abstract: A brachytherapy treatment apparatus is provided that includes a center catheter including proximal and distal ends defining a central longitudinal axis therebetween, the center catheter including a bend between the proximal and distal ends. The apparatus includes a pair of expandable catheters including pathways extending between the proximal and distal ends thereof, the expandable catheter distal ends coupled to the distal end of the core member. An actuator is coupled to the expandable catheters adjacent expandable portions that is movable relative to the center catheter for moving the expandable portions between a collapsed configuration wherein the expandable portions extend substantially parallel to the center catheter and an expanded configuration wherein the expandable portions bow away from one another substantially within a curved plane aligned generally with a bend of to the center catheter. A balloon is provided adjacent the expandable portions and surrounding a portion of the catheters.

Abstract: A force transducer is coupled to a distal portion of a shaft of a surgical instrument. The force transducer includes proximal and distal portions, radial ribs, and a plurality of strain gauges. The radial ribs form a plurality of through passages. The surgical instrument further includes a flush manifold that receives a liquid from a proximal portion of the shaft, and that directs the liquid along a first subset of through passages of the plurality of through passages toward the distal portion of the force transducer. A plenum at the distal portion of the force transducer collects the liquid from the first subset of through passages and redirects the liquid back toward the proximal portion of the shaft along a second subset of through passages of the plurality of through passages different from the first subset of through passages.

Abstract: A changeable positioning device for dental drilling comprises a base, a guide body and a positioning block. The base comprises a top end, a bottom end, a first outer wall, a first inner wall, a first guide groove, at least one first recess and at least one second recess. The at least one protrusion can be slidably fitted with the at least one first recess and the at least one second recess, thereby the second guide groove of the guide body will not be synchronously moved with a drill during drilling toward the axial direction of the guide body. The distance between the two extension portions is smaller than the diameter of the second inner wall at the same plane that is perpendicular to the axis of the guide body so that the drill will not deviate from the guide groove, thereby increasing the stability and precision of drilling.

Abstract: A dental wedge for inserting into the interproximal space between adjacent teeth comprises a first and second sidewall comprised of a shape memory material, including a nickel-titanium alloy, wherein the dental wedge is in a first, resting state when outside of the interproximal space and transforms to a second, operational state when the dental wedge is interested into the interproximal space between adjacent teeth and exposed to a first transformation stimulus, namely exposure to the higher temperature in the interproximal space. The expansion force generated by the dental wedge when in the second, operational stage is sufficient to secure a dental matrix against the tooth being restored and to separate the tooth being restored and adjacent tooth to expand the interproximal space.

Abstract: Disclosed are endodontic filling materials and methods. A method for filling a dental root canal may include providing a hydrosetting filling material and inserting the hydrosetting filling material into the dental root canal, the material setting in the root canal to form a biocompatible filling. The hydrosetting filling material comprises a hydrogel former and a filler. The hydrogel former is at least one of a reactive organic hydrogel formers, an inorganic hydrogel formers, and a non-reactive organic hydrogel formers, and the filler is at least one of a self-hardening and a non-hardening filler. Plural filling material precursor compositions that collectively contain hydrogel formers and fillers may be provided.

Abstract: A pocket orthodontic bonding pad for attaching orthodontic attachments to teeth wherein the orthodontic attachment is mechanically secured within a bonding pad pocket with a design that allows a slight buffering flexibility under masticatory stress and ease of removal of the orthodontic attachment. Upon removal of locking tabs the orthodontic attachment may be removed with minimal force, and the remaining bonding pad polished from the teeth with ease, which is most advantageous for brackets that tend to break upon removal and create high stress forces upon tooth structure. The ease of removing orthodontic attachments allows maximum bonding strengths.

Abstract: An implant fixture is disclosed. The implant fixture contains an elongated shaft section, and a head section, wherein the head section contains at least one concave area for bone growth therein.

Abstract: A conversion abutment that cements onto one-piece dental implants that convert the one-piece implant use to a retrievable screw retained implant use in retaining complete dentures, hybrids, partial dentures, or fixed screw retained crowns or bridges, allowing the flexibility to retain and remove these restorative prostheses. These conversion abutments can be fabricated as angled conversion abutments to be used with single or multiple implants placed at various angulations. The conversion abutment system consists of three parts: a cementable conversion abutment (straight or angled), a coping (short or extended), and an occlusal screw. The bottom part (or apical portion) of the implant conversion abutment will cement over the one-piece implant in use, while the top (or coronal portion) will allow a screw to fit through a coping into the implant conversion abutment, screwing the prostheses into place.

Abstract: An implant comprising two internal anti-rotational features. One anti-rotational feature is adapted to engage a driving tool, while the other anti-rotational feature is adapted to engage an abutment. An implant abutment system is provided with an angled abutment adapted to mate with one of the anti-rotational features. A second, straight abutment is adapted to engage with the other anti-rotational feature. An abutment is provided with resilient fingers to interface with the implant and provide tactile and audible feedback indicating when the abutment is properly seated. An abutment screw extends through the abutment and engages the implant bore distal of the stem of the abutment. The abutment screw limits axial movement of the abutment relative to the implant. A driving tool comprising one of at least retention structure and visual alignment indicia is provided to facilitate screwing the implant into a patient's bone.

Abstract: A dental articulator apparatus and method of forming dental casts utilizing a dental articulator having pivotally connected upper and lower arms that each have a ball socket which receives a ball at the outer end of a respective model anchor, the opposed end of which is cast into a dental model. The model anchor ball is adjustably secured in the ball socket of the articulator arms by a set screw coupled with a rotatable magnetic extension rod that are installed, removed, advanced, and retracted as a unit and allow relative rotation between the set screw and the extension rod to facilitate fitting and positioning the ball in the socket when the set screw is loosened, and eliminate manually installing and positioning separate small shims and plungers that can be accidentally dropped and lost.

Abstract: A dental superstructure with integrated spacers including a main body and at least one integrated spacer. The superstructure is intended to be connected to the at least one osseointegrated dental implant through connection between the integrated spacer and the osseointegrated dental implant. A manufacturing method thereof is also provided.

Abstract: A method comprises: bringing a plasma-treated liquid having an oxidizing power into contact with an object in an area; and mixing water and the plasma-treated liquid which remains in the area after the plasma-treated liquid is brought into contact with the object.

Abstract: The present invention relates to a device and a method for the application of composites in tooth cavities. The device consists of a spray gun with integrated lighting for light-polymerizable composites, a measuring unit and a control unit. The composites are applied under controlled, precisely dosed exposure to polymerization light. According to the invention, the composite initially runs onto the walls of the cavity or onto previously introduced filling material and then, as a result of the light exposure, is transformed into the gel state. Thus, a large part of the polymerization shrinkage of the composite occurs while the composite is still plastically deformable so that any formation of gaps is compensated by the composite continuing to flow. It is only at this point in time that a sufficiently high dosage of light is applied for complete curing to occur.

Abstract: An applicator for dispensing a therapeutic agent to an animal including a housing including first and second sections coupled together, the first and second sections defining a channel therebetween that includes at least one outlet; a hub integral with the first section and extending therefrom, the hub defining a conduit; and a bent path connecting the conduit to the channel. In accordance with this embodiment, the conduit, the bent path and the channel are fluidly connected.

Abstract: The invention discloses an implant. The implant may include a first flap and a second flap. The first flap may further include a first portion, a second portion and a transition region. The first portion may be configured to be attached proximate a sacrum. The second portion may be configured to be attached to an anterior vaginal wall. The transition region lies between the first portion and the second portion. The second flap may be fabricated such that a portion of the second flap is configured to be attached to a posterior vaginal wall. The implant may be configured such that a value corresponding to a biomechanical parameter defining a biomechanical attribute of the portion of the first flap attaching to the anterior wall is different from a value of the biomechanical parameter defining the biomechanical attribute of the portion of the second flap attaching to the posterior wall.

Abstract: An anal incontinence treatment apparatus with an adjustable restriction device implanted in a patient, who suffers from anal incontinence. The device engages a portion of the colon or rectum of the patient to restrict the fecal passageway. A hydraulic adjustment device adjusts the restriction device to restrict or release the fecal passageway, i.e. to normally close the fecal passageway and open the fecal passageway when the patient wants to relieve himself or herself.

Abstract: The present invention relates to a monofilament with a segmented pie structure formed by conjugated spinning of degradable polymers and non-degradable polymers, a hernia mesh having improved flexibility and biocompatibility, and a preparation method of the monofilament. More specifically, the hernia mesh of the present invention having improved flexibility and biocompatibility is prepared using the monofilament obtained by conjugated spinning of degradable polymers and non-degradable polymers into a segmented pie form, to control it to be gradually degraded in the body, whereby the stiffness of the early stage is removed, and thereby the foreign body sensation is also removed.

Abstract: 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.

Abstract: A method of delivering a therapeutic device to a treatment area of a body lumen, the therapeutic device including a) a delivery member possessing at least one attachment part and b) a treatment membrane, includes wrapping the treatment membrane on the delivery member, attaching the treatment membrane to the attachment part of the delivery member, and moving the delivery member toward the treatment area, detaching the treatment membrane from the delivery member, and withdrawing the delivery member from the body lumen.

Abstract: A system for facilitating deployment of an endoluminal prosthesis may include a main tubular graft body including a proximal end opening, a distal end opening, a lumen, and a sidewall. A branch may extend from the sidewall and may include a first end opening, a second end opening, and a lumen. A fenestration may be disposed in the sidewall and positioned distal of the second end opening of the branch. A wire segment may include a proximal portion positioned proximal of the proximal end opening and a distal portion positioned distal of the distal end opening. The wire segment extend through the fenestration and through the lumen of the branch in a preloaded configuration.