Abstract: The invention relates to a heart valve regurgitation drum and optional closure disk and/or tubular stent to manage and provide levels of intentional regurgitation within an orthogonally delivered transcatheter prosthetic heart valve having a first inner flow control component/valve, a second inner regurgitation control component, and an outer annular support frame having compressible wire cells that facilitate folding flat along the z-axis and compressing the valve vertically along the y-axis, or orthogonally to the central axis of the flow control component, allowing a very large diameter valve to be delivered and deployed to the tricuspid valve from the inferior vena cava or superior vena cava, or trans-atrially to the mitral valve, the valve having a height of about 5-60 mm and a diameter of about 25-80 mm, without requiring an oversized diameter catheter and without requiring delivery and deployment from a catheter at an acute angle of approach.

Abstract: Medical delivery system for accessing a tricuspid valve via an inferior vena cava, including an outer guide catheter, an inner guide catheter and an interventional catheter. The first deflection portion of the outer guide catheter is steerable to define a first outer-guide-catheter curve and the second deflection portion of the outer guide catheter is steerable to define a second outer-guide-catheter curve and the first deflection portion of the inner guide catheter is steerable to define a first inner-guide-catheter curve.

Abstract: A prosthesis for implantation at a native semilunar valve includes a prosthetic distal valve, which includes a pliant material configured to collapse inwardly towards a longitudinal axis of the prosthesis during diastole, and to open outwardly during systole, and a distal fixation member configured to be positioned in a downstream artery of the subject. The apparatus also includes a proximal fixation member coupled to the distal fixation member, and configured to be positioned at least partially on a ventricular side of the native semilunar valve. The proximal fixation member is shaped so as to define a lattice that is shaped so as to define an intermediary portion that is coupled to the pliant material of the valve and diverges outwardly from the longitudinal axis, and a distal portion that is distal to the intermediary portion and diverges outwardly from the intermediary portion of the lattice. Other embodiments are also described.

Abstract: The active introducer sheath systems disclosed herein are expanded by activating a translation mechanism at the handle. The sheath has an inner cylindrical structure of comingled fixed and mobile elongate rods bound together by an attachment line. Activating the translation mechanism causes the mobile rods to move axially with respect to the fixed rods, changing the internal tension in the attachment line. Increased tension draws the fixed and mobile rods closer together, decreasing the diameter of the cylindrical structure. Decreased tension in the attachment line enables the fixed and mobile rods to move apart, increasing the diameter of the cylindrical structure. A prosthetic device, such as a prosthetic heart valve, can be routed through the expanded sheath and to the implantation site. During implantation, the sheath can be contracted back to its original outer diameter, and expanded again for retrieval of the delivery apparatus.

Abstract: An implant is configured to be coupled to first and second native leaflets of a native heart valve of a patient. The implant includes a proximal collar, a distal collar, and first and second clasps. Each of the first and second clasps has first and second tissue-engaging portions that are (1) disposed distal to the proximal collar and proximal to the distal collar, (2) movable, with respect to each other, to clamp one of the leaflets between the first and second tissue-engaging portions of the clasp, and (3) movable, when clamped to the leaflet, toward and away from a central longitudinal axis of the implant. Other embodiments are also described.

Abstract: An apparatus includes a needle having a bore and a distal tip, a pusher having a distal end, the pusher being disposed within the bore of the needle for movement between a delivery position within the needle and a deployed position distal to the distal tip of the needle, an elongate tissue anchor including a distal portion and a proximal portion separated by one or more hinges, and a suture disposed at least partially within the pusher and coupled to the elongate tissue anchor.

Abstract: The present invention relates to an auxiliary artificial valve for implantation in blood vessel of a mammal patient. The artificial valve is provided with at least a first moving part and a second moving part configured to move between an closed position and an opened position, and a casing comprising at least one hinge, wherein the at least first moving part and second moving part are configured to be movably attached to the casing by means of said at least one hinge.

Abstract: Provided is a functional, low-profile intercranial device (LID). The LID includes a base portion; at least one cavity associated with the base portion and configured to accept at least one functional component; and at least one conduit having a first end in communication with the at least one cavity. The at least one functional component includes a medicinal, electronic, or optic therapeutic. The at least one conduit is configured to accept the medicinal therapeutic and a second end configured to dispense the therapeutic.

Abstract: Provided is a functional, low-profile intercranial device (LID). The LID includes a base portion; at least one cavity associated with the base portion and configured to accept at least one functional component; and at least one conduit having a first end in communication with the at least one cavity. The at least one functional component includes a medicinal, electronic, or optic therapeutic. The at least one conduit is configured to accept the medicinal therapeutic and a second end configured to dispense the therapeutic.

Abstract: The invention is directed towards a process for implanting a cartilage graft into a cartilage defect and sealing the implanted cartilage graft with recipient tissue by creating a first bore down to the bone portion of the cartilage defect, creating a second shaped bore that is concentric to and on top of the first bore to match the shape and size of the cartilage graft, treating the first bore and the second shaped bore at the defect site with a bonding agent, treating the circumferential area of the cartilage graft with a bonding agent, inserting the cartilage graft into the defect site and wherein the superficial surface of the cartilage graft is at the same height as the surrounding cartilage surface. The first and second bonding agents may be activated by applying a stimulation agent to induce sealing, integration, and restoration of the hydrodynamic environments of the recipient tissue.

Abstract: The present disclosure generally relates to a sacroiliac joint coupler having a base plate and an angled plate for respective engagement with the sacrum and ilium are described herein. The sacroiliac joint coupler includes a bolt having a threaded distal end extending from a top face of the base plate and a fastener that couples the distal end of the bolt to the angled plate. In addition, the fastener may include a hinge or a locking ball.

Abstract: An expandable interbody spacer for the spine is provided. The interbody spacer includes a housing, a top endplate and a bottom endplate. An actuator is located inside the housing between the top and bottom endplates. A locking screw is configured to drive the actuator and move the endplates between collapsed and expanded configurations. Variations of the expandable spacer are provided in which the endplates move bilaterally outwardly into uniform and parallel expansion along the latitudinal axis, the endplates angulate about a pivot point along a longitudinal axis such that the distal end of the spacer increases in height relative to the proximal end, and the endplates angulate about a pivot along a lateral axis such that the height along one lateral side of the spacer increases in height relative to the other lateral side.

Abstract: A spinal implant device comprising a frame and a plurality of mechanical stiffness members extending from the frame, with the plurality of mechanical stiffness members being individually customized to provide a specific axial stiffness. The plurality of mechanical stiffness members may be coupled to the frame, and the plurality of mechanical stiffness members may be a plurality of wave-spring modules. A method of treating spinal disease includes determining actual spatial mechanical properties across a vertebral contact surface of a vertebra of a patient. The method may also include manufacturing a spinal implant device that has conforming spatial mechanical properties that are specific to the patient and that are based on the actual spatial mechanical properties of the vertebral contact surface. The method may include surgically implanting the spinal implant device against the vertebral contact surface such that the actual spatial mechanical properties and the conforming spatial mechanical properties align.

Abstract: An expandable implant includes an upper plate configured to receive a first anchoring member, an upper support mechanically coupled to the upper plate, a lower plate configured to receive a second anchoring member, and a lower support mechanically coupled to the lower plate. The implant further includes a control member including a shaft and configured to control movement between the upper support and the lower support, a front portion configured engage the upper support and the lower support and further configured to receive the head of the control member, and a rear portion configured engage the upper support and the lower support and further configured to engage a portion of the shaft, wherein turning the control member causes the front portion to move in a direction towards the rear portion, such that the upper support moves relative to the lower support in a direction away from the lower support.

Abstract: An electronically assisted artificial vertebral disc having an upper disc plate and a lower disc plate is disclosed. An actuator imparts movement to at least one of the upper and lower disc plates. A control device controls the actuator and the amount of movement between the disc plates. The actuator includes a plurality of either linear actuators or rotary actuators that are driven by electric motors in response to the control device. The control device includes at least a first sensor for detecting the position of the actuator and at least a second sensor for detecting the spatial orientation of at least one of the upper and lower disc plates. The control device also preferably includes a microprocessor that calculates the desired positions of the upper and lower disc plates and provides a control signal to the actuator to drive the upper and lower disc plates to their desired positions.

Abstract: A spinal interbody implant includes a shaft extending along and rotatable about a central axis. The shaft includes a first threaded region. The implant further includes a first link having a first end with first gear teeth. The first end of the first link is fixed at a first point relative to the central axis such that the first gear teeth engage the first threaded region.

Abstract: Interbody spacers are expandable horizontally and vertically by an application of axial force, and lockable in an expanded configuration. The spacers include support members interconnected to end bodies by pivotable link members. The spacers are introduced between vertebral bodies in a compressed configuration and expanded to fill the intervertebral space and provide support and selective lordotic correction. Graft material may be introduced into the expanded spacer. Provisional and/or supplementary locking means lock the spacers in the expanded configuration. Embodiments of the spacers include symmetrically and asymmetrically configured spacers. Methods of expansion include symmetric expansion or asymmetric expansion along each of two directions.

Abstract: Systems and methods of treating spinal deformity, including one or more intervertebral implants to be introduced laterally into respective intervertebral spaces, a plurality of bone screws introduced generally laterally into vertebral bodies adjacent to the intervertebral implants and/or the intervertebral implants themselves, and a cable dimensioned to be coupled to the bone screws and manipulated to adjust and/or correct the spinal deformity.

Abstract: An intervertebral implant may include an input for expanding at least two extendable support elements connected to a body at respective locations, such that the extendable support elements each apply a respective expansion force directed away from a surface of the body. Application of a single input force to the input may induce the extendable support elements to apply different amounts of expansion force. Alternatively or additionally, an intervertebral implant may include at least two portions connected together by a hinge for articulation about the hinge. In one aspect, the hinge may include at least two rigid links each pivotably connected to the two portions. In another aspect, a rigid link of the hinge may include a passageway for communicating a hydraulic fluid between the two portions. A locking system may be positionable into successive locked configurations by operation of a cam to prevent contraction of an extendable support element.

Abstract: An implant extractor including a shaft body and a telescoping push rod extending from the shaft body. An adjustor is engaged with the telescoping push rod for adjusting a length of the telescoping push rod. A support arm extends laterally away from the shaft body and a jaw assembly extends from the support arm. The jaw assembly includes a jaw moveable between a locking position and an unlocking position, and a rocker arm operatively engaged with the telescoping push rod and the jaw. The implant extractor provides a line of force spaced from and substantially parallel to an implant to be extracted. As a consequence, there is substantial clearance for an extension handle such as a C-frame or the like which is oftentimes needed to dislodge the implant from surrounding bone. In addition, the implant extractor is capable of gripping a wide range of sizes of hip stem implant trunnions.

Abstract: An instrument may be coupled to a multi-axis expandable intervertebral cage so that the cage may be inserted into an intervertebral space, expanded along multiple different directions, filled with bone graft, and locked with a fastener. The instrument may be part of an instrument set that includes auxiliary instruments to determine implant size, insert bone graft into the cage, and deliver the fastener.

Abstract: A selection system comprises a ring, a plurality of shims, a measurement device, and at least one glenoid component. The ring is configured to couple to a humerus. A shim of the plurality of shims is configured to couple to the ring. The measurement device is configured to couple to the shim. Each shim of the plurality of shims has a different height when coupled to the ring. The selection system generates measurement data to support the selection of at least one prosthetic component for a shoulder joint in a surgical environment. The shoulder joint geometry can be adjusted by changing shims, changing glenoid component or both. The selection system is removed after the selection of the final prosthetic components for the shoulder joint. The final prosthetic components are installed in the shoulder joint. The measurement device is placed in the shoulder joint and measurement data is generated to verify performance.

Abstract: A hip joint navigation system is provided that includes a base having at least one channel disposed therethrough for receiving a pin for mounting the base to the pelvis. A mount feature is disposed on a top surface. A registration jig is configured to couple with the base and to engage anatomical landmarks. In some aspects, a patient specific jig system for hip replacement is provided including an engagement surface formed to closely mate to acetabular bone contours of a specific patient and a registration feature configured to be in a pre-determined orientation relative to an acetabulum the patient when the jig is coupled with acetabular bone contours of the specific patient. In other aspects, methods of using the systems are provided.

Abstract: The walking canister system and method are for manufacturing a prosthetic socket. The system includes a rigid canister, a suspension bladder positioned within the rigid canister, and an outer chamber wicking material arranged in an outer chamber defined between the suspension bladder and the rigid canister. A foam insert includes a contoured exterior surface configured to transfer pressure through to an interior surface thereof to produce consistent surface contact with a residual limb, of a walking patient, having casting material thereon. An inner chamber wicking material is arranged in an inner chamber defined between the foam insert and the suspension bladder. An outer chamber vacuum port is in fluid communication with the outer chamber, and an inner chamber vacuum port is in fluid communication with the inner chamber. An outer chamber suspension sleeve is configured to extend from the residual limb and over the rigid canister.

Abstract: A positioning device for a stent includes a positioning member including a handle and an extension secured to the handle wherein the handle and the extension are coaxially connected, and an open end of the extension is provided with a hollow first magnetic member; and a stent inserted into a blood vessel and including a first stent member inserted into an artificial blood vessel, the first stent member being separated into two second stent members inserted into the artificial blood vessel wherein a diameter of the first stent member is greater than that of each second stent member, and a diameter of each second stent member is greater than that of the extension, the stent further comprising at least one second magnetic member on the first stent member proximate an open end thereof, the second magnetic member being configured to attach to the first magnetic member.

Abstract: An adjustable bendable sheath, which is configured to deliver a stent into a vessel, includes a bendable tube and a pulling wire. One end of the pulling wire is fixedly connected to one end of the bendable tube, while the other end of the pulling wire extends out of the bendable tube and into the bendable tube until the pulling wire extends out of the other end of the bendable tube. When the other end of the pulling wire is pulled, the pulling wire drives one end of the bendable tube to move close to the other end of the pulling wire, so as to bend the bendable tube. The present application further relates to a stent delivery device having an adjustable bendable sheath, which is capable of effectively releasing a stent at a lesion site of the vessel.

Abstract: A delivery device (1) for an endoprosthesis (2). The endoprosthesis (2) is preferably an endoprosthesis for treating an aneurysm. The delivery device (1) comprises an outer sheath (3) and an inner tube (4). The inner tube (4) is arranged within the outer sheath (3) and at least one restraining tube (5, 30). The restraining tube (5, 30) is for holding the endoprosthesis (2) in a compressed configuration. The restraining tube (5, 30) is arranged between the outer sheath (3) and the inner tube (4). The outer sheath (3), the inner tube (4) and at least one restraining tube (5, 30) are coaxial. The restraining tube (5, 30) includes at least one axial elongation (6) extending from a distal end portion of the restraining tube. The at least one axial elongation (6) is adapted to be laced through portions of the endoprosthesis (2).

Abstract: A stent delivery device for releasing a stent into a vessel. The stent delivery device includes a fixing assembly including a fixing member and a limiting member, wherein one end of the limiting member passes through the stent and abuts against the fixing member to lock the stent; and a releasing assembly including a movable member and a locking member connected to the movable member, wherein the movable member is connected to the other end of the limiting member, and the locking member is slidably connected to the movable member. When the locking member is in a first position, the movable member is fixed relative to the fixing member under the restriction of the locking member. When the locking member slides to a second position, the movable member can drive the limiting member to move away from the fixing member to release the stent.

Abstract: A joint orthosis assembly includes a web, an arm unit, a strap unit, and at least one fastening subassembly. The web has three web portions for being wrapped on an upper limb structure, a lower limb structure, and a joint between the upper and lower limb structures, respectively. The arm unit is retained on the web and includes two arms which are pivotally connected, and which are for being disposed at lateral sides of the upper and lower limb structures, respectively. The strap unit includes two straps each being wound about the web to be coupled between the two arms. The fastening subassembly is configured to permit an end of at least one of the straps to be turnably coupled to a corresponding one of arms.

Abstract: An orthopedic device comprises a frame assembly comprising a parallel frame member and a perpendicular frame member. Each of the parallel frame member and the perpendicular frame member are substantially elongate in shape, and each have a first end and a second end. The orthopedic device further comprises at least three primary extensions each having a mount end and a free end. The perpendicular frame member is coupled by the first end thereof to the parallel frame member along the length of the parallel frame member between the first end and the second end thereof. Each of the at least three primary extensions is adjustably disposed by the mount end thereof along the frame assembly.

Abstract: A waist, hip and pelvis adjustment belt includes a waist, hip and pelvis adjustment belt assembly and plural ore bodies distributed and accommodated in the waist, hip and pelvis adjustment belt assembly. When a user wears the waist, hip and pelvis adjustment belt assembly to have the effect of lifting and binding the user's waist and hip, the ore bodies in the waist, hip and pelvis adjustment belt assembly will release far infrared light to generate a resonance frequency to promote blood circulation of the user's lower limbs, and restore and adjust the user's pelvis and hip joint, so that the user's piriformis and nerve will not be pressed to achieve the effect of good functionality and structural stability.

Abstract: A method and device for limiting the displacement of a human body without restricting natural movements are disclosed. The device comprises a strip or cord, an anchor element on one end of the strip, and a hooking element on the other end of the strip. The anchor element is used to fix one end of the strip to a fixed or static surface/point. The hooking element, at the other end of the strip, is used to attach the device to a harness or the person's clothing. The method describes the use and attachment of the device. The main application of the method and device is to keep a child safe in a bed without the risk of falling out of bed, but applies to any person, lying down or sitting, regardless of age.

Abstract: A contact piece and a urine discharge device are provided. The contact piece includes a ring having inlet and outlet openings in communication with each other and an elastic fitting membrane having an end coupled to the ring in a sealed condition and an opposite end forming a membrane surface to cover the inlet opening. The membrane surface is formed with a second through opening. The elastic fitting membrane is made of a material having an extremely high elastic expansion/contraction rate and waterproofness. The contact piece is combinable with a urine conducting piece to form a urine discharge device. The expandability of the elastic fitting membrane allows the contact piece to be fit to a male sexual organ and the elastic fitting membrane is in complete engagement with the sexual organ to prevent urine leaking, while the elastic fitting membrane applies a proper pressing force to the sexual organ.

Abstract: A physiological fixed device includes a main body unit having a main body respectively provided on top and bottom surfaces thereof with an abutted portion for contacting a human body, which has at least one excretion collecting opening for excretion to fall into a collecting part and V-shaped cross sections corresponding to the physiological structure of the buttocks groove for good fitness, and an accommodating portion for accommodating a urine bag. An underclothing unit is connected with the main body unit for being positioned on the human body to locate the main body unit at the crotch, so that it is convenient for wearing and carrying, suitable for men and females with different physiological structures, useful for collecting feces and urine, and high in compatibility, thereby convenient and practical. This invention also provides an assembly of the aforementioned physiological fixed device and a collecting bag.

Abstract: A dental device adapted to provide forward relative positioning of a mandible of a patient including: a mandibular tray formed to the patient's mandibular dentition including a mandibular attachment wire encased within an outer circumference of the mandibular tray; a maxillary tray formed to the patient's maxillary dentition, the maxillary tray including a maxillary attachment wire encased within an outer circumference of the maxillary tray; and a pair of hinge devices coupled to the mandibular tray via the mandibular attachment wire and coupled to the maxillary tray via the maxillary attachment wire, each hinge device including a housing having an inner channel and a telescoping member movable within the inner channel to change a length of the hinge device to enable forward mandibular advancement, the telescoping member including precise circumferential grooves.

Abstract: A dental oral appliance for using inside an oral cavity, where the oral cavity has an upper row of teeth, a lower row of teeth, a tongue, and an upper jaw. The upper and lower row of teeth define a lingual side. The dental oral appliance includes a separating portion and a tongue supporting portion, where an upper teeth region is defined above the separating portion and a lower teeth region is defined underneath thereof. The upper teeth region is adjacently disposed around the upper row of teeth, and the lower teeth region is adjacently disposed around the lower row of teeth. The outer edge of the tongue supporting portion is connected to one side of the separating portion close to the tongue.

Abstract: A device for modeling a pessary is disclosed. A matrix of individually expandable balloons are mounted around a shaft, which holds fill lines for each balloon. The balloons are expandable with fluid to a desired volume and/or pressure, according to comfort and fit determined by real-time patient feedback. Because the volumes and the positions of the balloons are known, a calculation of the dimensions of the vaginal canal can be made, so that the matrix of expandable balloons models the vaginal canal.

Abstract: Systems and methods for manipulating the temperature of a surface are described. Described embodiments include thermal adjustment devices that may include a heatsink and that are operated in two or more modes of operation to apply a desired temperature to a user. In one operating mode the thermal adjustment device may apply a first temperature to an underlying surface while generating heat at a rate faster than the heatsink's heat dissipation rate. The thermal adjustment device may then apply a second temperature to reduce the rate of heat generation to be less than the heatsink's heat dissipation rate. These modes of operation may be applied cyclically to permit continuous operation of the thermal adjustment device. In some embodiments, the temperature profile applied when changing between the modes of operation may be selected such that the user experiences either a reduced, or substantially, neutral thermal sensation.

Abstract: Disclosed is an applicator device for an apparatus used in a localized cryotherapy treatment. The applicator device is configured, when positioned over a body area to be treated, to receive and to uniformly distribute across the entire area covered thereby a stream of medium, such as air, adjusted to a temperature equal to or above ?40 degrees Celsius (° C.) and directed, at a predetermined speed, via the applicator to the area to be treated, whereby a cold-induced thermal shock response is developed in skin and an underlying tissue within the area covered by the applicator. Related apparatus and a method are further provided.

Abstract: A cooling sheet is provided. The cooling sheet according to one embodiment of the present invention includes a moisture storage layer which stores therein moisture, an absorbing layer which is fused to one surface of the moisture storage layer to absorb the moisture and is applied with microcapsules containing a functional material, and a water repellent layer which is fused to the other surface of the moisture storage layer to be in contact with skin, prevents the moisture from escaping and absorbs air from outside. Accordingly, it is possible to provide a cooling sensation using heat of evaporation when in contact with skin while preventing moisture from escaping to the outside along seam lines.

Abstract: A method for solid water particle treatment of eye, ear, and nose ailments detects and treats ailments in the eyes, ears, and nose through a procedure of capturing infrared images of the Meridian pathway near the eyes, ears, or nose, and then administering a solid water particle solution to help repair the Meridian pathway. The efficacy of the solid water particle solution is determined by capturing an initial image and a subsequent image of the Meridian pathway near the eyes, ears, or nose. The skin temperature of both images is visually indicated in a thermal coloring or white-hot spot. If the temperatures detected in the subsequent infrared images decrease, the Meridian pathway of the eyes, ears, or nose is improving. Thus, the status of the eyes, ears, or nose is determined based on changes in skin temperature at the Meridian pathway approximate to the eyes, ears, or nose.

Abstract: The present invention is directed to a device for the access and delivery of cells or other materials to the subretinal space. The device of the present invention accesses the subretinal space via the trans-scleral side. This is an ah externo approach. The device includes two stacked layers, surrounded by a flexible outer surface and an OCT-sensor integrated guide needle. The device is configured to be flexible, such that it conforms to the natural curvature of the eye as it is advanced to the subretinal space. After the device is in place, the flexible outer surface is configured to protect the delicate tissue of the retina and choroid, while there is also easy passage of the material or cells to be delivered between the two stacked layers.

Abstract: Provided are multi-wavelength phototherapy devices, systems and methods for the treatment of a disorder or disease, including multi-wavelength low level light therapy (“PBM”), in particular to multi-wavelength PBM and other phototherapy systems and methods for improving functionality in and/or restoring functionality to a cell and/or tissue through the coordinated and targeted delivery to the cell or tissue of two or more doses of light having distinct wavelengths, wherein the two or more doses of light, when delivered in a coordinated fashion, can stimulate the activity of two or more light sensitive factors that, when activated, provide and/or enhance a desired target cell functionality. Ophthalmic phototherapy devices, systems, and treatment methods to expose an eye to selected multi-wavelengths of light to promote the healing of damaged or diseased eye tissue.

Abstract: An anterior chamber maintainer (ACM), which is to be utilized in connection with maintaining physiological intraocular pressure during intraocular surgery is disclosed and is seen to comprise an axially elongated tubular member which is adapted to be fluidically connected at a first end to a supply of balanced salt solution (BSS) for introduction into the anterior chamber of an eye so as to maintain adequate intraocular pressure while performing any intraocular surgery. A second opposite end of the anterior chamber maintainer (ACM) is provided with a sharply pointed end for insertion through a paracentesis formed within the limbus region of the eye, and a deformable bulbous portion is interposed between the first and second ends such that as the second end passes through the paracentesis, the bulbous portion will diametrically deform and then diametrically expand, after also passing through the paracentesis, thereby trapping the anterior chamber maintainer (ACM) within the anterior chamber of the eye.

Abstract: A surgical cannulated blade instrument includes a blade portion having a pointed end, a top surface, and a bottom surface opposite the top surface, an increasing diameter portion having a diameter which increases in a direction away from the pointed end, and a cannula portion having a lumen opening at a location between the pointed end and the increasing diameter portion. An eye surgery method includes incising a cornea of an eye using a blade portion of a surgical cannulated blade instrument to create an opening in the cornea, injecting injectable into an anterior chamber of the eye through the opening by a lumen of the surgical cannulated blade, and stabilizing the eye by engaging an increasing diameter portion of the surgical cannulated blade with the opening.

Abstract: The present disclosure relates to a fog-reducing apparatus for eye protection equipment. For example, the fog-reducing apparatus includes a filter-pump system that provides air through one or more flexible hoses and across a lens of eye protection equipment. In certain implementations, the fog-reducing apparatus includes one or more nozzles (e.g., interchangeable nozzles) that provide directional air flow across the lens. Depending on the nozzle and/or an air flow controller, the fog-reducing apparatus can provide variable amounts of air flow and adjustable air flow direction as may be desired. In addition, the nozzle can attach to one or more components of the eye protection equipment, such as a lens, shield, or hood via one or more attachment mechanisms. Further, the nozzle can be inserted through an air vent or other hole into the eye protection equipment.

Abstract: The disclosure relates to an earpiece configured to be at least partially inserted into an ear and comprising a core comprising a material that during insertion of the earpiece into the ear is deformable above a transition temperature and non-deformable below the transition temperature. The disclosure also relates to a method of manufacturing the earpiece. The disclosure further relates to a method of customizing the earpiece.

Abstract: A According to the present disclosure, there is provided a compression stocking for a hemiplegia patient worn on the hemiplegia patient's arm or leg, including: a main body having an observation portion configured to observe a corresponding body portion so as to check a vascular lesion of the patient, in which the main body has different compression degrees depending on portions of the arm or the leg. According to the present disclosure, it is possible to correct and treat the acute unilateral limb problem by wearing the compression stocking on the arm or leg requiring treatment of the hemiplegia patient, prevent thrombus by compressing the arm or leg with different pressures in a state where the compression stocking for a hemiplegia patient is worn on the hemiplegia patient's arm or leg, and check the vascular lesion of the patient through the observation portion formed at the end thereof in a state where the compression stocking for a hemiplegia patient is worn on the hemiplegia patient's arm or leg.

Abstract: A method of manufacturing a swab for collecting a biological specimen includes extruding a first portion of a stem with at least one of a first taper and/or a first wall thickness, and extruding a second portion of the stem with at least one of a second taper and/or a second wall thickness.

Abstract: A disposable diaper that includes a traditional outer shell and a replaceable insert is disclosed. The insert can be removed without taking the outer shell off the wearer. The insert may be replaced as many times as desired by the user, thereby greatly reducing the amount of waste associated with disposable diapers. It should also be noted that the disposable diaper may be manufactured and marketed as a unit, the unit including both the outer shell and the replaceable insert. Alternatively, the replaceable inserts may be manufactured and marketed as a separate product.