Abstract: A multi-chamber balloon for a nuclear implant has an elastomeric membrane defining inner and outer chambers integral with a valve body. The valve body includes a core portion and sealing membrane for sealing the inner and outer chambers. An assembly for manufacturing the multi-chamber balloon includes a balloon mandrel which may be dip coated in a silicone dispersion to create an elastomeric membrane for the inner and outer chambers integral with the valve body. The elastomeric membrane formed on the mandrel is partially inverted to form a coaxial elastomeric structure with the smaller inner chamber disposed within the larger outer chamber. The valve is incorporated into the inner and outer chambers to form a unitary structure.

Abstract: Disclosed are devices, methods and/or systems for intervertebral and intradiscal implants deployed within the body of a patient, including improved interbody devices having internal and/or external characteristics that facilitate use of the implant in a plurality of different orientations.

Abstract: A system and method for electrical stimulation in an orthopedic implant that includes at least one implantable component with an implant body, a plurality of electrodes, and implant circuitry is effective to convert an external wireless power transmission to an electrical current and effective to control the plurality of electrodes; and at least one non-implant with a power source, and transmitter circuitry to generate the electromagnetic field that couples with the implant circuitry.

Abstract: A spinal implant system is provided for bridging an intervertebral space between vertebral bodies bordering the intervertebral space. The spinal implant system includes at least one adjustable end cap and a spinal implant. The end cap can be used with additional end caps and/or the spinal implant. Multiple end caps can be stacked on top of one another, and one end cap can be attached to a first end of the spinal implant, and another end cap 10 can be attached to a second end of the spinal implant. Thus, one or more of the end caps can be attached to either end of the spinal implant.

Abstract: A system for use during surgical procedures. The system includes an implant and a tool. The implant combines a modular adjustable cage and a shim that locks the cage into position, after the cage has been adjusted to its final position and at its final height, in situ. The tool combines an expander and an inserter. A related method of using the system is also provided.

Abstract: A bone graft delivery system can include an elongate tube and a handle having a trigger and a ratcheting mechanism. The trigger is actuated to deliver bone graft material through the tube. The bone graft delivery system can further include a distal tip at a distal end of the tube. The tip has one or more openings to deliver the bone graft material to a desired location and includes a surface suitable to act as a rasp for decorticating bone. A method for delivering bone graft material to a desired surgical location includes providing a bone graft delivery device, positioning the device adjacent the surgical location, decorticating bone, and delivering bone graft material to the surgical location.

Abstract: An orthopaedic surgical instrument for positioning an acetabular prosthetic component in a patient's surgically-prepared acetabulum includes a surgical tool configured to be coupled to the acetabular prosthetic component, and a gravity-based position indicator removably coupled to the surgical tool. The position indicator includes a first marking indicating a first position of the acetabular prosthetic component, and a second marking indicating a second position.

Abstract: A flexible plastic, resin or polymer material forming a trial plate for use is surgery of bones including spine and extremities. The trial plate having at least one radio opaque region and guides for positioning. A kit may be provided containing at least one flexible trial plate.

Abstract: Provided is a resin-impregnated rolled fabric sock with one or more opposed pairs of tails for ease of applying the sock to the limb, the sock being useful for preparing casts or forms on limbs. The sock is provided rolled upon itself down the outer side from the open end to the closed end and along the long axis of the sock. The tails are incorporated into the roll, however an exposed end of each tail remains external to the roll. In an embodiment, the resin-impregnated, rolled sock is provided in a sealed moisture impermeable container. Also provided are methods of use.

Abstract: A medical apparatus is provided for use in manufacturing a plaster impression of limb stump, in particular of a lower stump, wherein the apparatus comprises a pressure vessel with a fluid container of pressure chamber for receiving or storing a fluid being under pressure, wherein the pressure vessel comprises a wall made of a first material, wherein the wall limits the an interior of of the pressure vessel against an exterior, wherein the pressure vessel comprises an insertion opening for the insertion of a limb stump into the interior of the pressure vessel and a fluid-tight membrane made of a second materials, which is arranged to form or limit the fluid container or the pressure chamber. An upper section of the membrane is preferably releasably fastened at or to the pressure vessel by a connector.

Abstract: A stent device includes generally cylindrical rings aligned along a longitudinal axis, and interconnected by interconnecting members. Each interconnecting member includes a first coupling end, a second coupling end, and an elongate portion therebetween. The first coupling end, the elongate portion, and the second coupling end combine in either a first orientation or a second orientation, which are substantially mirror images. For each interconnecting member, the first coupling end can intersect with a midpoint of a transition region of a substantially repeating curved segment on one of the rings, and the second coupling end can intersect with a midpoint of a curved segment of a different and immediately adjacent ring. The interconnecting members can be arranged in rows extending longitudinally along the device. Along each row, consecutive interconnected members alternate between the first orientation and the second orientation. A cover may be provided over the stent device.

Abstract: A method may include deploying a stent such that at least one opening of the stent is aligned with a tissue surface within a body of a patient, manipulating a tissue portion through the at least one opening of the stent, and securing the tissue portion with respect to the opening of the stent to prevent migration of the stent. Another general aspect of the present disclosure includes a stent. The stent may have a body including a plurality of struts, a covering extending to an end of the body, the end being a proximal end of a distal end, and an anchor secured to the end of the body, where the anchor includes an opening that is exposed with respect to the covering.

Abstract: A stent includes a high radial force segment and a highly flexible segment, where the diameters of the high radial force segment and the highly flexible segment are substantially the same. The stent may further be placed with an additional stent segment, where the additional stent segment has a radial force similar to the radial force of the highly flexible force segment.

Abstract: A stent includes a high radial force segment and a highly flexible segment, where the diameters of the high radial force segment and the highly flexible segment are different. For example, the stent may be formed from a tube having varying diameters as it extends distally combined with increased strut density to achieve increased flexibility distally while reducing loss of radial stiffness. The stent may further be placed with an additional stent segment, where the additional stent segment has a radial force similar to the radial force of the highly flexible force segment.

Abstract: The present disclosure comprises devices, systems, and methods having an inverted sheath configured to cover, and in some instances constrain, a medical device and to retract through eversion, thus enabling the deployment of medical device at the treatment site. A constraining sheath can evert hydraulically. A constraining sheath can be configured to neck down a medical device to achieve a lower delivery profile. Furthermore, a constraining sheath can comprise a balloon to expand or positionally or structurally adjust a medical device.

Abstract: The present disclosure relates generally to the field of medical devices. In particular, the present disclosure relates to devices and methods for controlled delivery of a stent, such as a self-expanding stent, and more particularly for controlling the full deployment of a stent in incremental steps from a sheath and for controlling the reconstrainment of a stent in incremental steps within a sheath.

Abstract: A self-expanding element delivery apparatus includes a catheter having an inner lumen, a self-expanding element, and a delivery wire disposed within and extending through the inner lumen and the self-expanding element. The self-expanding element has a proximal, distal, and an intermediate portion. The element has anchor members, a compressed configuration fitting within the inner lumen, and an expanded configuration dimensioned larger than the catheter. The delivery wire also has proximal and distal portions, an intermediate portion, a dual function bump member disposed approximate to the intermediate portion, and a pusher bump member disposed approximate to the proximal portion of the delivery wire. A bump member distance between the dual function bump member and the pusher bump member is such that so that only one of the dual function bump member and the pusher bump member can contact one of the anchor members.

Abstract: A delivery system and method for implanting a stent graft includes a flexible sheath that defines openings distributed longitudinally and wherein substantial alignment of the openings along a longitudinal axis of a guidewire catheter radially constrict the flexible sheath. The flexible sheath includes at least one fenestration. A ligature extends through the openings of the flexible sheath and causes the openings to be substantially aligned, thereby constraining the flexible sheath. The ligature is proximally retractable from the openings to thereby release the flexible sheath from a radially constricted configuration.

Abstract: The present disclosure relates to a support system for patients recovering from medical procedures, including from total knee replacement surgery. The disclosed system may include a foot support unit which supports a patient's feet, where the foot support may have leg grooves separated by a divider and a tapered height. The foot support may be placed in a patient's bed. Additionally hip support wedges may be placed beneath a patient's hip, where the hip supports provide the benefit of counteracting a leg's natural tendency to rotate outwards. The disclosed foot support and hip wedges promote proper alignment and in that way provide comfort and assist in recovery.

Abstract: A knee brace including upper and lower pairs of struts articulately interconnected by two ligaments respectively located inside two joint capsules, wherein the upper and lower pairs of struts are respectively removably connected to opposite ends of the two ligaments by upper and lower removable fasteners located inside the two joint capsules, and wherein each joint capsule has a hole to access one of the upper and lower fasteners thereby allowing each of the upper and lower pairs of struts to be disconnected from one another by a single fastener.

Abstract: An orthopedic walking boot includes a housing configured to encompass at least a user's foot, a mechanically adjustable ramp insert comprising a ramp surface and disposed in the housing, and an adjusting mechanism configured to adjust an elevation angle of the ramp surface. The mechanically adjustable ramp insert includes a base, a threaded shaft secured to the adjusting mechanism at a first end and configured to rotate with the adjusting mechanism, a first slider nut comprising internal threads, a bracket in physical contact with the ramp surface, a first support coupled to the first slider nut at a first end and to the bracket at a second end, and a second support coupled to the base at a first end and to the bracket at a second end.

Abstract: A soft robotic spinal orthosis includes a control system having at least one processor, a plurality of adjustable pressure fluid bladders to provide at least one variable supporting force to a torso of a user, a plurality of supports to secure the fluid bladders to the torso, at least one sensor to detect a position of the torso, and at least one pressure device to increase and decrease a fluid pressure of the fluid bladders.

Abstract: Head-and-neck immobilization devices may include a yoke sized and shaped to contact a person's back and shoulders. Two head immobilization pads may be sized and shaped to respectively contact opposing sides of the person's head, each of the two head immobilization pads connected to the yoke at a single location by a respective selectively rotatable, selectively fixable connection and independently fixed in place to immobilize the person's head responsive to the rotatable, selectively fixable connection to the yoke in a fixed mode.

Abstract: A patient support apparatus comprises a support structure comprising a head end, a foot end, a base, and a patient support deck. The patient support deck comprises a fowler section at the head end and a foot section at the foot end. The fowler section is capable of articulating relative to the base. The patient support apparatus further comprises a pediatric support module comprising a seat section disposed between the fowler section and the foot section. The pediatric support module is integrated into the patient support deck and comprises a lid and a body.

Abstract: An ostomy appliance including an ostomy pouch with a filter and a center pleated panel to protect the filter, facilitate deodorization and deter ballooning.

Abstract: Systems and methods provide for holding surgical drain evacuators in inelastic expandable pouches. Particularly, apparatuses and methods include or utilize garments for supporting and protecting surgical drain evacuators and surgical drains include straps or belts for attaching the garment to a patient. The garments include one or more expandable pouches configured to receive a surgical drain evacuator, wherein the expandable pouch is formed of a flexible inelastic material.

Abstract: A urine collection device includes a collection member extending from a proximal end to a distal end. The proximal end includes an opening that provides access to an internal cavity of the collection member. The internal cavity includes a first chamber in fluid communication with a second chamber. The urine collection device includes a spacer in the second chamber, a first attachment member extending from a bottom wall of the collection member at the proximal end., a second attachment member extending from a top wall of the collection member at the proximal end, and an outlet for egressing urine from the internal cavity of the collection member. The first attachment member defines an aperture. The collection member is suitable to (i) direct urine from the first chamber to the second chamber and (ii) direct the urine in the second chamber distally toward the outlet.

Abstract: A non-invasive urine collection device is disclosed that can be used by both male persons and female persons. For example, the urine collection device is designed such that through orientation and/or deformation, the urine collection device may be configured to seal around the human pelvic area to sanitarily and non-invasively collect urine. The collection device comprises a funnel with a drain as a first end and a receptacle opening at a second end opposite the first end, a handle on one side, and a flexible ring seal along the perimeter of the receptacle opening. The flexible ring seal, shape of the receptacle opening, and the angle of the funnel wall in relation to the receptacle opening and funnel drain is such that the collection device can be used in either a handle up or handle down orientation.

Abstract: An apparatus for improving dexterity of the bare hands in cold temperatures includes heating pads 10 disposed on the forehead, cheeks and forearms. The heating pads 10a, 10b, 10c on the forehead and cheeks stimulate the trigeminal nerve area to increase blood flow to the fingers. The heating pads 10d, 10d on the forearms 24, 24 increase the temperature of the blood flowing to the hands. Thermocouples 32 in each heating pad 10 are connected to a set-point controller 28.

Abstract: A device for producing control data for a laser device for the surgical correction of defective vision. The device produces the control data such that the laser emits the laser radiation such that a volume in the cornea is isolated. The device calculates a radius of curvature RCV* to determine the control data, the cornea reduced by the volume having the radius of curvature RCV* and the radius of curvature being site-specific and satisfying the following equation: RCV*(r,?)=1/((1/RCV(r,?))+BCOR(r,?)/(nc-1))+F, wherein RCV(r,?) is the local radius of curvature of the cornea before the volume is removed, nc is the refractive index of the material of the cornea, F is a coefficient, and BCOR(r,?) is the local change in refractive force required for the desired correction of defective vision in a plane lying in the vertex of the cornea, and at least two radii r1 and r2 satisfy the equation BCOR(r=r1,?)?BCOR(r=r2,?).

Abstract: The invention relates to a method for forming curved cuts in a transparent material, in particular in the cornea, by the creation of optical perforations in said material using laser radiation that is focused in the material. The focal point is displaced three-dimensionally to form the cut by lining up the optical perforations. The focal point is displaced in a first spatial direction by a displaceable lens and said focal directions, in such a way that it follows the contours of the cut, which lie on a plane that is substantially perpendicular to the first spatial direction.

Abstract: Methods for treatment of dry eye and other acute or chronic inflammatory processes are disclosed herein. One method includes administering a drug delivery implant to a patient in need thereof, the drug delivery implant comprising one or more Rock inhibitors and/or one or more Wnt inhibitors, the patient having a medical condition selected from the group consisting of dry eye, lichen planus, arthritis, psoriasis, plantar fasciitis, pars planitis, scleritis, keratitis, chronic meibomian gland inflammation, optic nerve neuritis, uveitis, papillitis, diabetic neural pain, diabetic retinopathy, a cataract, a side effect occurring after refractive surgery, a side effect occurring after corneal transplant, a side effect occurring after retinal detachment surgery, and combinations thereof. The administration of the drug delivery implant to the patient treats the medical condition, reduces the symptoms associated with the medical condition, enhances nerve regeneration, and/or alleviates the medical condition.

Abstract: A method of treatment is disclosed herein. The method includes administering to a patient in need thereof a polymer implant device containing a biocompatible drug, or a plurality of nanoparticles or microparticles conjugated with the biocompatible drug, the biocompatible drug comprising one or more Rock inhibitors, one or more Wnt inhibitors, one or more integrin inhibitors, and/or one or more glycogen synthase kinase 3 (GSK-3) inhibitors, the patient having a medical condition selected from the group consisting of dry eye, glaucoma, retinal detachment, retinal degeneration, age-related macular degeneration, a cataract, uveitis, a corneal genetic disease, postoperative inflammation, immune-related inflammatory processes, diabetic retinopathy, a side effect occurring after cataract surgery, a side effect occurring after refractive surgery, and combinations thereof.

Abstract: The present disclosure describes systems and methods for selectively constraining an orientation of a portion of a surgical tool system relative to another. Example surgical tool systems may include a surgical tool having at least one movable component, at least one actuation component, and a surgical tool attachment. The surgical tool attachment may be operable selectively to engage and disengage the moveable component so as to to prevent movement of the movable component relative to the surgical tool in an engaged configuration and to permit movement of the movable component relative to the surgical to in a disengaged configuration, respectively. In the engaged configuration, a dynamic component of the surgical tool system may be fixed relative to the surgical tool, and, in a disengaged configuration, the dynamic component may be freely movable relative to the surgical tool.

Abstract: An insertion tool, systems, and methods for use with lacrimal implants are herein provided. An insertion tool is disclosed that includes an inserter tip with a static pin at a distal end configured to be placed in a bore of a lacrimal implant and a mechanical coupling to receive a handle at a proximal end of the inserter tip; and, a handle coupled to the inserter tip at a distal end of the handle and a plunger at a proximal end of the handle, wherein the plunger is configured to release the inserter tip from the handle. The static pin of the inserter tip is de-coupled from the lacrimal implant after placement in a lacrimal canaliculus without mechanical force from the insertion tool.

Abstract: A shunt 10 for implantation in the human body for treating ocular disorders related to disorders of intraocular or intracranial pressure by providing for flow of aqueous fluid in the anterior chamber A of the eye and cerebrospinal fluid in the subarachnoid space B surrounding the optic nerve C. The shunt has a proximal end 12 which is implanted in the ocular anterior chamber and a distal end 14 which is implanted in the subarachnoid space. The shunt has a two-part construction, including a flexible distal tube 18 and a rigid proximal tube 20. The distal tube has a distal stop formation 26 near the distal end 14 which is located in the subarachnoid space upon implantation of the distal end, resisting withdrawal of the shunt. The proximal tube has a curved portion which conforms to the anatomical curvature of the ocular globe.

Abstract: Shunt devices and a method for continuously decompressing elevated intraocular pressure in eyes affected by glaucoma by diverting excess aqueous humor from the anterior chamber of the eye into Schlemm's canal where post-operative patency can be maintained with an indwelling shunt device which surgically connects the canal with the anterior chamber. The shunt devices provide uni- or bi-directional flow of aqueous humor into Schlemm's canal.

Abstract: The present disclosure provides a system for femtosecond ophthalmic surgery in which a measuring device and a camera generate data that is processed and used to create an enhanced pictorial representation based on the actual positions of the suction ring and the eye. The pictorial representation may include a graphic relating to ophthalmic surgery, such as for a flap or an incision. The disclosure further provides a method for docking a suction ring in femtosecond laser ophthalmic surgery, which includes observing and generating data relating to the position of the suction ring, generating data relating to a pictorial representation of the suction ring and the eye, processing the data relating to the observed position and the pictorial representation to generate an enhanced pictorial representation, and presenting it during surgery. The pictorial representation may include a graphic relating to ophthalmic surgery, such as for a flap or an incision.

Abstract: Antimicrobial dressings for prevention and mitigation of biofilm and bacterial infection by an applied electric current are provided. Methods of making the dressings and methods of applying an electric current to promote the wound healing process are also disclosed.

Abstract: A negative pressure wound closure system and methods for using such a system are described. Preferred embodiments of the invention facilitate closure of the wound by preferentially contracting to provide for movement of the tissue. Some embodiments may utilize a stabilizing structure with dissolvable portions.

Abstract: A negative pressure wound therapy system includes a wound dressing and a suction device configured to be in fluid communication with the wound dressing via a conduit to channel a fluid between at least the wound dressing and the suction device. The suction device includes a vacuum connection configured to be coupled to the conduit, a vacuum pump, an analog electronic pressure sensor in electrical communication with the vacuum pump, and a passive valve assembly. The passive valve assembly is in fluid communication with (1) the vacuum pump, (2), the analog electronic pressure sensor, and (3) the vacuum connection, and is configured to maintain the vacuum pump in fluid communication with the vacuum connection within a predefined pressure range, and to passively inhibit fluid communication between the vacuum pump and the vacuum connection outside of the predefined pressure range.

Abstract: According to an aspect of the disclosure, a protective film for application to a portion of an individual's body, a method for applying a protective film to a portion of an individual's body, and an apparatus with a protective film for application to a portion of the individual's body are provided.

Abstract: The present invention relates to a nonwoven acquisition distribution layer comprising: a) layered carded webs wherein the first layer comprises a carded web with high denier fibers wherein the denier is greater than about 5 d and a second layer comprising a carded web with low denier fibers wherein the denier is less than about 5 d and is positioned just below and in direct contact with the first layer; and b) a deflection layer comprising a fibrous nonwoven web wherein the fibrous nonwoven web has at least one component comprising meltblown, said meltblown having a basis weight of from about 15 gsm to about 50 gsm and having an air permeability of from about 45 ft3/min/ft2 to about 350 ft3/min/ft2; and wherein the deflection layer is positioned just below and in direct contact with said second layer of said layered carded web.

Abstract: A method for producing a multi-layered absorbent articles is disclosed. At least two of the layers include a colored region.

Abstract: A conveying device comprises: a plurality of holding mechanisms attached to a rotary shaft; a speed-changing mechanism which changes the angular speed of each of the plurality of holding mechanisms; a first cover extending from a first holding mechanism toward a second holding mechanism, such that the first cover covers a gap between the two holding mechanisms from an outside thereof in a radial direction of the rotating shaft; and a second cover extending from the second holding mechanism toward the first holding mechanism such that the second cover covers the gap from the outside thereof in the radial direction, and overlapping with the first cover. The two covers have lengths enough to be able to overlap with each other in the radial direction in a state in which the two holding mechanisms are furthest apart from each other.

Abstract: This disclosure relates to a combination of a sensing device and a charging system. The sensing device is configured to be applied to a surface of an absorbent article for sensing a characteristic of moisture in the absorbent article, and it is configured such that a transmitter for transmitting data from the sensing device is attached or attachable to the sensing device. The charging system is configured to charge a transmitter battery, and it is configured such that a transmitter, which is attached or attachable to the sensing device, is also attachable to the charging device.

Abstract: A disposable wearing article which enables the liquid absorbent structure to fit the body stably, without a shift in position of the waist opening edge part when worn. A liquid absorbent structure further has an end flap positioned between a front-end edge of the liquid absorbent structure and a front-end edge of an absorbent core. A front waist region has a stretchable sheet extending inward in a vertical direction Y from a waist opening edge and overlapping with the end flap, a plurality of waist elastic members extending in a lateral direction X and overlapping with at least the end flap, a first region positioned between the waist opening edge and the front-end edge of the liquid absorbent structure, and a second region including the stretchable sheet and the waist elastic members, at an inner side in the vertical direction Y of the front-end edge of the liquid absorbent structure.

Abstract: The present technology relates to an absorbent product for attachment to an article of clothing The absorbent product comprises a wearer-facing surface and a garment-facing surface opposite the wearer-facing surface. The absorbent product comprises a main body, wherein the main body comprises: a central absorbent core; an external envelop placed around the central core and having a front extremity and a rear extremity; a first attachment line located at the front extremity of the external envelop; and a second attachment line located at the rear extremity of the external envelop; wherein the first attachment line and the second attachment line are for attachment of the absorbent product to the article of clothing; and wherein the absorbent product is free of means for adhesively attaching the garment-facing surface to the article of clothing.

Abstract: A disposable absorbent article is described. The disposable absorbent article has a topsheet, a backsheet, and an absorbent core disposed between the topsheet and the backsheet. A carded staple fiber nonwoven having a basis weight of between about 50 grams per square meter (gsm) and about 100 gsm, includes a blend of absorbing fibers, stiffening fibers and filler fibers. The carded staple fiber nonwoven has a pore volume radius mode of between about 60 ?m and about 120 ?m.

Abstract: A wearable article comprising: a main body comprising an outer cover layer and a backsheet attached to the skin-facing surface of the outer cover layer; and a ring-like elastic belt comprising a front belt and a back belt; the backsheet comprising a printed main artwork observable from the garment-facing side of the article. The main artwork exists in the vicinity of the proximal edge of the central panel of at least one of the front and back belts, extends from at least one of the front and back central panels into the crotch panel; and comprises a belt area artwork displayed on the central panel and a crotch area artwork displayed on the crotch panel. The relationship of the opacity of the outer cover layer to the opacity of the central panel overlayed on the garment facing side of the backsheet is defined herein.