Abstract: An atherectomy device with an exchangeable drive shaft is disclosed, having a drive shaft gear at a distal end of the exchangeable drive shaft for meshing engagement with a prime mover gear on the output shaft of the prime mover. The exchangeable drive shaft is inserted into an opening at the distal end of the handle housing and moved axially in a proximal direction. Surface features on at least the prime mover housing and the engageable drive shaft help to align the drive shaft gear with the prime mover gear for meshing engagement.

Abstract: A surgical instrument is designed for clamping, cutting, and/or joining tissue. This surgical instrument includes a handle portion, an elongate portion extending distally from the handle portion, first and second jaw members disposed adjacent a distal portion of the elongated portion, a shaft movable upon actuation of the handle portion, and a knife bar operatively coupled to the shaft. At least one of the jaw members is movable with respect to the other between an open position and an approximated position for engaging body tissue therebetween. The knife bar has a curved profile and moves along at least one of the jaw members upon movement of the shaft.

Abstract: A handheld device for repeated local puncture of human or animal skin, comprising a housing having a handle, a drive device in the housing supplied with a rotating movement about an axis of rotation by a driveshaft, a conversion mechanism coupled to the driveshaft to convert rotating movement into a driving movement along a driving movement direction, and a puncture device which is arranged in the housing and as a puncture needle, which is arranged on a needle shaft that can be moved back and forth repeatedly along a path of movement together with the puncture needle and is connected to the conversion mechanism, wherein the conversion mechanism has a rod crank device, and the stroke executed by the puncture element in moving back and forth is adjustable by altering a relative position between an axial direction of the axis of rotation and the direction of the driving movement.

Abstract: A stylet for insertion within a cannula interior of a needle is disclosed. The stylet includes a solid elongated shaft having a proximal end adapted for engagement with a needle hub, and a distal end having a surface modified profile. The surface modified profile increases the penetration force required to penetrate human skin. The ratio of the penetration force of a stylet having an unmodified distal end to the stylet having a surface modified profile is at least 1:1.4, or greater. The surface modified profile may be a roughened surface, a buffed surface and/or a blunted surface. The surface modified profile may include a yieldable material disposed over at least a portion of the distal end. A needle assembly having a stylet having a surface modified profile is also disclosed.

Abstract: An epidural space identification device to identify when a tip of a needle used for epidural anesthesia enters an epidural space that includes a barrel formed in a cylindrical shape and communicatively connected to a needle section, a plunger formed in a cylindrical shape, retractably inserted into the barrel, and having an air hole communicating with an inside of the plunger, and an expansible member having an expansible part provided at a front end part of the plunger and bulging inside of the plunger with a positive pressure generated by pushing the plunger while air discharge from a needle side is regulated.

Abstract: The invention relates to a surgical apparatus, in particular a navigation probe for localizing and treating lesions in a brain, comprising: a body member (10) having an anterior end (20), a posterior end (30) and at least one groove (60, 62) extending for a particular length in a longitudinal direction of the body member (10) between said anterior end (20) and said posterior end (30); a saddle (70) adapted to securely hold a medical device, the saddle (70) being placed on said body member (10) and having at least one grip (74, 75, 76) that extends into said at least one groove (60, 62) so as to mount the saddle (70) on the body member (10) moveable in said longitudinal direction; and a means for maneuvering said body member (10).

Abstract: Access needles and methods of using the needles are set forth in this disclosure. The needles can include a handle and a cannula having a proximal end operatively connected to the handle, a distal end, and a lumen extending through the body of the cannula. A protective sheath may surround the cannula. Further, a stylet may be removably disposed within the lumen of the cannula. The stylet includes a piercing tip at a distal end and a flexible body length extending proximally from the piercing tip to the handle. The flexible body of the stylet provides a path of fluid communication through the lumen of the cannula such that a contrast fluid can effectively pass through the lumen of the cannula. Methods of introducing cannulas to target locations within a body of a patient are also set forth in this disclosure.

Abstract: Exfoliating heads with an abrasive surface are disclosed for use with a personal care appliance. The personal care appliance is configured to oscillate the exfoliating head to provide improved smoothing and exfoliation of a subject's epidermis with or without the antecedent application of skin care formula. The oscillating action of the exfoliating head may be rotational, translational, or a combination thereof. In use, the personal care appliance oscillates the abrasive surface of the exfoliating head over a subject's skin in order to remove dead skin from the subject's epidermis. The exfoliating heads may be used to treat rough skin conditions, such as calluses or corns, which have developed on a patient's hand or foot.

Abstract: A device for accessing and distending a joint comprises a distraction structure having a generally tapered distal portion adapted to penetrate a tissue region and create an access space within a joint. The distraction structure also includes a lumen extending from a proximal surface to a distal portion. The device further includes a distention structure deployable through the lumen and adapted to exert a force between a first joint surface and a second joint surface and create a working space. The distention structure may, in some embodiments, include an elongate member having a proximal end, a distal end, and a lumen extending along at least a portion of the length of the elongate member, a first expandable region deployable from a first substantially collapsed position to a second substantially expanded position, the first expandable region adapted to exert a force between the first joint surface from the second joint surface.

Abstract: Clamping devices and methods for external fixation systems include a post component having a yaw axis and a clamping system secured to the post component and rotatable about the yaw axis. The clamping system includes a outer jaw and a inner jaw having an inner surface facing the outer jaw. The outer and inner jaws together form an opening for receiving a fixation element of the external fixation system. The inner jaw and outer jaw have a roll axis alignable with a longitudinal axis of the fixation element. The clamping system and post component are rotatable about the roll axis. The inner jaw also includes a cylindrical outer-facing surface. The devices also include a base component having a cylindrical concave surface having a pitch axis. The concave surface of the base component interfaces with the cylindrical outer facing component on the inner jaw. The outer and inner jaws being rotatable relative to the base and the post component about the pitch axis.

Abstract: Fixation device for pins to be attached to an external fixation system, comprising: a first attachment or clamp comprising a first pair of opposite jaws (2) for housing at least one pin, said first pair of jaws (2) being formed by a lower jaw element (20) and an upper jaw element (30); a second attachment comprising a second pair of opposite jaws (6) that define together at least one seat for housing a rod of the external fixation system; a first clamping screw (4) for clamping the first pair of jaws (2) in order to lock in position the at least one pin, said first clamping screw (4) screwing along a screw axis (X); one of said jaw elements (30) of the first pair of jaws (2) having at least one appendix (33) on its outer edge that is shaped to interact with a corresponding recess (23) made on the other jaw element (20) of the first pair of jaws (2) so that the only possible sliding will be along the screw axis (X) of the first clamping screw (4) a second clamping screw (5) for clamping the second pair of jaws

Abstract: A pair of bone plates adapted for attachment to cranial bone segments, the cranial plates being mounted to a distraction mechanism such that the cranial plates can be separated gradually in very small increments. Each of the cranial plates is mounted to the distraction mechanism with a ball and socket connector assembly, such that each of the plates can move in multiple directions and orientations relative to the distraction mechanism to better accommodate a convex, planar or concave surface topography presented during the distraction procedure.

Abstract: An external fixing device for the treatment of bone fractures includes a first member, a second member, a central body arranged between the first member and the second member, a first ball joint for the articulated connection of the first member with the central body, a second ball joint for the articulated connection of the second member with the central body, locking means operatively associated to the first ball joint and with the second ball joint, respectively, the locking means being suitable for allowing/preventing the articulation of the first member and second member with respect to the central body, wherein the first member includes a first clamp, the second member includes a second clamp and the central body includes a third clamp for connection of the external fixing device to respective fractured bone portions to be treated.

Abstract: The present invention relates to a medical instrument for applying a bone plate fixing device which comprises a first bone contact element with a rod-shaped connecting member protruding therefrom and defining a longitudinal direction and a second bone contact element which is movable on the connecting member towards the first bone contact element, characterized by a feed apparatus comprising a feed element for application to the second bone contact element, a guide element with a proximal and a distal end for guiding movement of the feed element and a feed mechanism for moving the feed element in the distal direction relative to the guide element.

Abstract: A dynamic fixation medical implant having at least two bone anchors includes a longitudinal connecting member assembly having at least one transition portion and cooperating outer sleeve, both the transition portion and sleeve being disposed between the two bone anchors. The transition portion includes a rigid length or rod having apertures therein and a molded plastic length that extends through the apertures, thus attaching the plastic length to the rigid length. The sleeve surrounds the transition portion and extends between the pair of bone anchors, the sleeve being compressible in a longitudinal direction between the bone anchors.

Abstract: A receiver for engaging a bone stabilizing element includes a receiver portion connectable to the stabilizing element, and a base portion connectable to a bone of a patient. The base portion may connect to the bone with a bone screw, for example a polyaxial bone screw, and the receiver portion may connect to the stabilizing element, for example a rod, using a set screw. The receiver portion and the base portion are slideably connected to each other, coupled and constrained in relative movement, by overlapping portions. Axial rotation between the receiver portion and the base portion is enabled by changing the relative dimensions of overlapped portions.

Abstract: The present invention generally is directed toward a spinal fixation system whereby a coupling element allows the physician to selectively lock or unlock either the connection between the coupling element and a fastener, such as to allow for repositioning of the coupling element, or the connection between the coupling element and an elongate rod. The locking or unlocking of these connections may be made independently and as desired by the physician.

Abstract: An anchoring member for a polyaxial bone anchoring device includes a bone anchoring section having a first end, a second end, a core having a first portion with a constant cross-sectional area, and a bone engagement structure on at least a portion of the core, a head, wherein a central axis extends through respective centers of the head and the first and second ends of the bone anchoring section, and a neck, the neck having an outer surface that is asymmetric with respect to the central axis, wherein a first cross-section of the neck perpendicular to the central axis includes a portion of the neck where the outer surface of the neck is at a minimum distance from the central axis, wherein a cross-sectional area of the first cross-section of the neck is at least the cross-sectional area of the first portion of the core of the bone anchoring section.

Abstract: The present invention provides spinous process implants and associated methods. In one aspect of the invention, the implant includes at least one extension with a superior lobe pivotally connected to an inferior lobe, such as by a hinge, to allow unfolding of the at least one extension from a folded position to an unfolded position. In certain aspects, the folding extension may include fasteners to facilitate engagement with the spinous processes to provide both a flexion stop as well as an extension stop. The fasteners may have corresponding bores to allow the fasteners to reside in the bores to provide a compact profile for implantation. In another aspect of the invention, the implant is introduced to the surgical site using a lateral or paramedian approach and associated tools to facilitate the same.

Abstract: Devices, systems, and methods for inserting a vertebral stabilization member, such as a rod. The insertion device includes an outer guide tube, a pin assembly including a pin and a pusher member extending therethrough. The insertion device is configured to actuate a rod between a first orientation and a second orientation angled with respect to the first orientation in order to position the rod in an appropriate location for attachment to bone.

Abstract: An articulating rod inserter is configured for use in delivering a fixation rod to an orthopedic fixation system through a cannula or tower. The articulating rod inserter is releasably coupled to a rod and can move the rod from a generally aligned configuration, wherein the longitudinal axes of the rod and rod inserter are generally aligned, to an angled configuration, wherein the longitudinal axis of the rod is at an angle to the longitudinal axis of the rod inserter. The rod is inserted into the patient through a first tower and then articulated to a second tower such that the rod extends between two or more fixation devices.

Abstract: Minimally invasive methods and devices for introducing a spinal fixation element into a surgical site in a patient's spinal column are provided. In general, the method involves advancing a spinal fixation element in a first, lengthwise orientation along a pathway extending from a minimally invasive percutaneous incision to a spinal anchor site. As the spinal fixation element approaches the spinal anchor site, the fixation element can be manipulated to extend in a second orientation, which is preferably substantially transverse to the first orientation, to position the fixation element in relation to one or more spinal anchors.

Abstract: Embodiments are generally directed to an apparatus for reducing a rod into an orthopedic fixation device. An embodiment provides a rod-reducing apparatus. The rod-reducing apparatus may comprise a housing comprising a threaded through bore. The rod-reducing apparatus further may comprise a reduction shaft comprising a shaft portion and a through bore in the shaft portion, wherein the shaft portion may be configured to be received within the threaded through bore of the housing. The locking cap driver may comprise a locking cap driver comprising a shaft portion that may be configured to be received within the through bore of the reduction shaft, wherein a distal end of the shaft portion may be configured for attachment to a locking cap assembly.

Abstract: A bone plate includes first and second longitudinal sides, a plurality of through holes longitudinally displaced in the bone plate between the first and second longitudinal sides, and a plurality of tubular guide elements coupled relative to the plurality of through holes. Plate bending tools are provided. Each includes a handle having a first end, a second end, and a longitudinal axis, and an end effector coupled to the first end of the handle. The end effector includes a retaining arm that is provided with a bore having a bore axis extending transverse relative to the longitudinal axis and a fulcrum. The bore is sized to received a portion of a tubular guide element coupled to the bone plate such that the retaining arm can stably engage the tubular guide element. The fulcrum is adapted to bear against one of longitudinal sides of the bone plate.

Abstract: A method for repairing a bone includes attaching a bone plate to the bone. The bone plate includes an upper surface, a bone-contacting surface, and at least one hole extending between the upper surface and the bone-contacting surface. The method also includes inserting at least a portion of a delivery device into the at least one hole. The delivery device includes at least one of an osteobiologic material, a graft material and a pharmacological substance. The method further includes injecting the at least one of the osteobiologic material, the graft material and the pharmacological substance into the bone and through the at least one hole.

Abstract: A system and method for the surgical correction of a bunion deformity allows for correction of a bunion deformity. The method includes: drilling a hole across a first metatarsal and through a second metatarsal; placing a tube from outside the first metatarsal through the hole across the first and second metatarsals; pushing a first button through the tube until the first button exits the tube through a medial side of the second metatarsal; flipping the first button to engage the first button against the second metatarsal and applying a lateral tension on the suture strand; manually pushing the first metatarsal and the second metatarsal together to correct intermetatarsal angular deformity; pulling free ends of the suture strand of the suture-button construct to advance a second button of the suture-button construct and to engage the second button against the first metatarsal; and securing the second button against the first metatarsal.

Abstract: Expandable fixation assemblies, expandable cranial fixation assemblies, and expandable intervertebral implant assemblies are provided for securing structures to bone and for securing bones and/or bone segments with respect to each other. An expansion member can be moved through at least a portion of an expandable fixation body, thereby causing expansion of the expandable fixation body, such that bone engagement features of the expandable fixation body engage surrounding structure, such as bone.

Abstract: An interphalangeal fusion implant comprising a threaded shank and a head, the head having a body portion having first and second laterally spaced fins, each of which has a plurality of axially spaced serrations, some of the serrations terminating at the laterally outermost ends at substantial single points. A driver for implanting an interphalangeal fusion implant comprising an elongate body, a receiving formation having at least two radially extending outward projections, and a pear shaped portion extending along a central axis of the body. A method of fusing a first phalanx and a second phalanx using an interphalangeal fusion implant.

Abstract: An instrument for extracting a pin from a substrate, such as a bone mass, which comprises a first lever arm with a body part having a channel in which a free end of a pin can be received, a second lever arm which can pivot relative to the first lever arm, a gripping member within the body part by which the pin can be gripped to retain the pin in the channel, and a terminating member mounted on the body part having an end face and two side walls which extend along opposite sides of the body part. The terminating member has a slot provided in a portion of the end face and which extends along a portion of at least one of the two side walls configured to guide the free end of the pin into the instrument prior to being received into the channel.

Abstract: A method and system for continuously delivering cryotreatment to a treatment device. In one embodiment, the system may include a first PID circuit in the fluid delivery line and a second PID circuit in the fluid return line, and the first and second PID circuits may operate simultaneously to continuously provide coolant to a cryotreatment device during the inflation phase, ablation phase, and warming (or thawing) phase while providing for temperature adjustment. Alternatively, the system may include a bypass line by which coolant may bypass the subcooler system and be delivered to the cryotreatment device at non-ablation temperatures during the inflation phase. During the ablation phase, coolant may flow through the subcooler system.

Abstract: Cryotreatment devices and methods of ablating tissue within the body are disclosed. A cryotreatment device in accordance with an exemplary embodiment of the present invention includes an elongated member having one or more needle-like ablation tips configured to induce necrosis at a target site within the heart. A cooling fluid such as a cryogen may be injected through a lumen extending into the distal portion of the device. The ablation tips can be configured to pierce and ablate surrounding tissue, blocking electrical stimuli that can cause fibrillations or other arrhythmias of the heart. The device may also include means for controlling the transmural depth at which the ablation tips are inserted into the cardiac tissue. Methods of forming a contiguous line of conduction block in accordance with the present invention are also disclosed.

Abstract: A high frequency electrosurgical power generator configured to produce electrical power at a frequency of about 1 to about 14 MHz and preferably having an essentially sinusoidal waveform with a voltage level up to 1,000 Vrms, and a current level up to 5 Amps. The output of the high frequency electrosurgical power generator is connected to an electrosurgical tool configured to receive the voltage and current produced by the electrosurgical power generator and deliver the voltage and current to an electrosurgical site. The output of the electrosurgical generator preferably is an essentially sinusoid waveform with a frequency between about 3 MHz and about 8 MHz, up to about 700 volts rms, up to about 2 amps, with a total power of up to 1,000 watts.

Abstract: A method for mitigating leakage in an RF electrosurgical generator includes delivering an RF signal from an RF electrosurgical generator to an electrosurgical electrode by way of a patient box; providing a balanced and symmetrical shielded transmission line coupling said electrosurgical generator disposed in a first housing to said patient box disposed in a second, different housing; providing a common mode choke in said patient box, said common mode choke including an output winding and a return winding, said output winding and said return winding spaced apart and in parallel to maintain a desired impedance, said output winding comprising a wire carrying said RF signal as an output signal and said return winding carrying a return signal from a return electrode; and directing a common mode signal from said RF signal to said common mode choke thereby blocking said common mode signal.

Abstract: A usage key card is adapted to be handled separate from a tissue treatment device. The usage key card has a storage medium formatted to contain an identification code, which is unique to the usage key card. The usage key card is also adapted to be read by a reader separate from the device. The storage medium is also formatted, when inserted into the reader, to retain data generated pertaining to operation of the device.

Abstract: The present disclosure relates to devices, systems and methods for evaluating the success of a treatment applied to tissue in a patient, such as a radio frequency ablative treatment used to neuromodulate nerves associated with the renal artery. A system monitors parameters or values generated during the course of a treatment. Feedback provided to an operator is based on the monitored values and relates to an assessment of the likelihood that a completed treatment was technically successful. In other embodiments, parameters or values generated during the course of an incomplete treatment (such as due to high temperature or high impedance conditions) may be evaluated to provide additional instructions or feedback to an operator.

Abstract: A system for the manufacture of an end effector assembly which is configured for use with an electrosurgical instrument configured for performing an electrosurgical procedure is provided. The system includes a photolithography module that is configured to etch one or more pockets on a seal surface of the seal plate. A vacuum module is configured to raise, transfer and lower a spacer from a location remote from the pocket(s) on the seal plate to the pocket on the seal plate(s). An adhesive dispensing module is configured to dispense an adhesive into the pocket on the seal plate. An optical module is configured to monitor a volume of the adhesive dispensed within the pocket and monitor placement of the spacer within the pocket.

Abstract: A treatment instrument includes a first clamping surface, a second clamping surface configured to cooperate with the first clamping surface and to clamp a living body tissue, a pressure application member provided on one of the first and second clamping surfaces, and configured to apply a pressure to the living body tissue in a line shape by causing the first and second clamping surfaces to relatively approach each other, and a moving mechanism provided on the first clamping surface, and configured to move the first clamping surface in a manner to apply tensile forces to the living body tissue, clamped between the first and second clamping surfaces, in directions deviating away from a direction along a line formed on the living body tissue by the pressure application member.

Abstract: A system for controlling operation of a radiofrequency treatment device to apply radiofrequency energy to tissue to treat tissue to create lesions without ablating the tissue. The system includes a first treatment device having a plurality of electrodes. The electrodes are maintained in axial alignment and fixed radial spacing in retracted and extended positions. The device includes a basket having a plurality of arms. The arms are maintained in a fixed radial spacing in the collapsed position of the basket.

Abstract: A catheter for the high-frequency therapy of body lumens has a flexible shaft tube of preferably biocompatible plastic material, which is connected to a distal end piece in the region of the distal end of the catheter. A proximal part of the distal end piece, that projects into the distal part of the shaft tube, forms a damping connection to the distal end of the shaft tube, which is secured by a distal electrode which is drawn on to the external peripheral surface of the shaft tube, by the distal electrode exerting a radially inwardly acting clamping force on the damping connection.

Abstract: An electrosurgical balloon includes an inflatable balloon body formed of a non-conductive substrate material. One or more electrodes are disposed on an exterior surface of the balloon body. The electrodes can include a pair of bipolar electrodes, and the balloon body can have at least one fluid outlet hole configured to provide fluid to the pair of bipolar electrodes. A second inflatable balloon body can be disposed inside the first inflatable balloon body. The electrosurgical balloon can be incorporated into a catheter assembly, in which the electrosurgical balloon is a balloon electrode tip at a distal end of a catheter.

Abstract: Systems and methods for forming a lesion on an endocardial tissue of a patient's heart involve placing an ablation assembly inside of the heart and adjacent to the endocardial tissue, and placing a guiding assembly outside of the heart. An ablation assembly includes an ablation element and a first attraction element, and a guiding assembly includes a second attraction element. First and second attraction elements can be attracted via magnetism. Techniques involve forming an ablation on the cardiac tissue of a patient's heart with an ablation element of the ablation assembly. Optionally, techniques may include moving the second attraction element of the guiding assembly relative to the patient's heart, so as to effect a corresponding movement of the ablation element of the ablation assembly.

Abstract: The present invention encompasses apparatus and methods for mapping electrical activity within the heart. The present invention also encompasses methods and apparatus for creating lesions in the heart tissue (ablating) to create a region of necrotic tissue which serves to disable the propagation of errant electrical impulses caused by an arrhythmia.

Abstract: Methods for treating polycystic ovary syndrome with therapeutic ovarian neuromodulation and associated systems and methods are disclosed herein. Polycystic ovary syndrome can be associated, for example, with a condition including at least one of oligo/amenorrhea, infertility, hirsutism, obesity, metabolic syndrome, insulin resistance, and increased cardiovascular risk profile. One aspect of the present technology is directed to methods that at least partially inhibit sympathetic neural activity in nerves proximate an ovarian artery of an ovary of a patient. Sympathetic drive in the patient can thereby be reduced in a manner that treats the patient for the polycystic ovary syndrome. Ovarian sympathetic nerve activity can be modulated along afferent and/or efferent pathways. The modulation can be achieved, for example, using an intravascularly positioned catheter carrying a therapeutic assembly, e.g.

Abstract: A device positionable in a cavity of a bodily organ (e.g., a heart) may discriminate between fluid (e.g., blood) and non-fluid tissue (e.g., wall of heart) to provide information or a mapping indicative of a position and/or orientation of the device in the cavity. Discrimination may be based on flow, or some other characteristic, for example electrical permittivity or force. The device may selectively ablate portions of the non-fluid tissue based on the information or mapping. The device may detect characteristics (e.g., electrical potentials) indicative of whether ablation was successful. The device may include a plurality of transducers, intravascularly guided in an unexpanded configuration and positioned proximate the non-fluid tissue in an expanded configuration. Expansion mechanism may include helical member(s) or inflatable member(s).

Abstract: Systems and methods for assessing tissue contact, including positioning a plurality of electrodes adjacent a tissue region; delivering radiofrequency energy to the plurality of electrodes, wherein the delivered radiofrequency energy is sufficient to ablate at least a portion of the tissue region; obtaining a plurality of impedance measurements from the plurality of electrodes during the delivery of the radiofrequency energy; calculating a change in the impedance measurements for each of the plurality of electrodes over a pre-determined time period; comparing the calculated change for at least one of the plurality of electrodes to the calculated change in at least one other of the plurality of electrode to determine if there is significant variation in the calculated changes; and terminating the delivery of radiofrequency energy to at least one of the plurality if there is significant variation in the calculated changes.

Abstract: A system for use with a microwave antenna includes a microwave antenna configured to deliver microwave energy from a power source to tissue and a sensor module in operative communication with the power source and configured to detect a reflectance parameter. The system further includes a jacket adapted to at least partially surround the microwave antenna to define a fluid channel between the jacket and the microwave antenna. A plurality of fluid distribution ports are defined through the jacket and are in fluid communication with the fluid channel to permit the flow of fluid through the jacket. The system further includes a fluid pumping system operably coupled to the power source and configured to selectively provide cooling fluid to the fluid channel for distribution through the fluid distribution ports based on the reflectance parameter.

Abstract: The present application relates to a cutting head for a device for cutting hair. The cutting head has a laser generator (2) and an optical system (3). The optical system is configured to focus a laser beam (4) generated by the laser generator and direct the laser beam along an optical axis (16) across a cutting zone (8) in the cutting head. The laser generator and optical system are configured such that, in a focus spot (15) of the laser beam, a dimension of the focus spot, a power density of the laser beam and the numerical aperture of the laser beam are such that, when a hair is received in the cutting zone, the power output of the laser generator is minimized while ensuring that, for a predetermined exposure time, the hair received in the cutting zone is cut by optical absorption. The present application also relates to a device for cutting hair and a method of controlling a cutting head for a device for cutting hair.

Abstract: The disclosure relates to a multifunctional sharps container having a first dispensing compartment for storing unused sharps and a second compartment for receiving used sharps. The first and second compartments are separated by a generally liquid impermeable partition fixed to the walls of the container. In addition, the first and second compartments are provided with apertures and structures for conveying the sharps, out of and into the compartments respectively, which are functional in at least two orientations of the container.

Abstract: A surgical system for and a method of identifying an incision site includes a surgical system having an intra-urethral probe and a template. The probe has a distal end opposite of a proximal end that is insertable into a urethra of a patient. The probe is sized and configured to prevent the proximal end of the probe from entering a bladder of the patient. A proximal end portion of the probe is magnetized to a first polarity. The template is sized for placement between an anus and a scrotum of the patient. The template includes a magnetic region magnetically attractable to the first polarity of the probe.

Abstract: A system for evaluating patency includes a light sensor (128) positionable relative to a blood vessel to receive light from the blood vessel and convert the light into an image signal. A photo-plethysmography (PPG) interpretation module (115) is configured to receive the image signal and output pixel values in an image representing PPG information. An image generation module (148) is coupled to the PPG interpretation module to receive the pixel values and generate a PPG map to be output to a display for analysis.