Abstract: A system for replacing a hip joint can include a first acetabular cup formed of a first material and having a first inner diameter and a first thickness. A second acetabular cup can be formed of a second material and having a second inner diameter and a second thickness. A first femoral hip prosthesis can include a first femoral head that is alternately accommodated by either of the first or second acetabular cups. A bearing can be adapted to be interposed between the first femoral head and one of the first or second acetabular cups. The first and second inner diameters can be the same. The first thickness can be less than the second thickness. The first material can be distinct from the second material.

Abstract: The invention relates to an acetabular cup (4) and a cup insert (3) for a hip joint prosthesis (12), wherein the cup insert (3) is coupled to the acetabular cup by means of a clamping cone (5) of a conical clamping device in the equatorial region (7) of the two components (3, 4) and, in the unloaded state of the cup insert (3), a gap (8) is provided between the two components (3, 4) below the clamping cone (5) to the pole (6), said gap being delimited by the radial contours of the two components (3, 4). In order to reduce the tensile stresses in the cup insert, the radial contours of the two components (3, 4) have identical geometric elements in the same order, starling front the lower cone end (9) to the pole (6), and tangential or substantially tangential transitions exist between the geometric elements.

Abstract: The present invention provides a femoral prosthesis for a femur which can enable or allow deep knee flexion without creating excessive tension in the ligamentous structure of the knee. The femoral prosthesis includes an internal non-articulating surface, an external articulating surface, a medial condyle and a lateral condyle. The height of the medial condyle is less than the height of the lateral condyle. A proximal-posterior tip of the medial condyle is rounded and is shifted inwards relative to the native level of the proximal-posterior region of the femur bone to facilitate knee flexion. A method of mounting a femoral prosthesis on a femur is also described.

Abstract: An orthopedic joint prosthesis may include a first component, a bearing component, and a third component. The first component has a base and a keel protruding from the base to extend into a first bone. The keel's longitudinal axis is offset from a geometric center of the base. The base has a first articular surface and the bearing component has a second articular surface shaped to articulate with the first articular surface. A feature unitary with the first component reversibly attaches to the bearing component. The bearing component has a third articular surface shaped to articulate with a fourth articular surface on the third component. A distraction feature of the bearing component is shaped to provide alignment and/or distraction between the first articular surface and the fourth articular surface during insertion of the bearing component into a joint space between the first and second bones.

Abstract: A surgical instrument for use in an orthopaedic arthroplasty procedure includes a shaft having a first end and a second end and an impactor head disposed at the second end of the shaft. The impactor head includes first and second spaced ends, two spaced impaction surfaces disposed at the second end, and a cavity disposed between the impaction surfaces. The cavity is adapted to accommodate posterior-stabilizing spines of at least a first tibial implant component and a second tibial implant component having a size different than a size of the first tibial implant component. Each of the impaction surfaces includes a first section with a contour that conforms to a contour of a bearing surface of the first tibial implant component and a second section with a contour that conforms to a contour of a bearing surface of the second tibial implant component.

Abstract: A tibial tray component includes a tibial tray portion with a post portion protruding from a bone-contacting side of the tibial tray portion. The tibial tray portion may include ribs extending along the bone-facing side in areas of high stress during the gait cycle. The post portion may include at least one fin projecting outwardly from the post portion and extending along a portion of the length of the post portion. A cut block assembly includes a cut block and at least one pin. The cut block may include several mounting locations for the pin. The pin may include an anti-rotation portion and a tapered free end.

Abstract: The invention discloses a support element for humeral implant comprising a central body extending along an axis and at least three arms extending outwardly from the central body, the arms being transversal to said axis and bearing a ring element at their ends opposite to said central body, wherein at least a first and a second pair of arms form different angles.

Abstract: In an artificial joint that includes a head assembly attached by taper fit to a proximal portion of a surgically implanted stem, it may become necessary to surgically remove the head assembly. A puller can simultaneously apply a force distally to a non-peripheral portion of a proximal side of the head assembly and proximally to several locations spaced apart around a circumference of the distal side of the head assembly. In some examples, the proximal side of the head assembly includes a plug disposed at the non-peripheral portion. The puller can force the plug into contact with the proximal end of the stem, then apply the distal force through the plug to the stem. In other examples lacking a plug, the non-peripheral portion of the head can deform or break in response to the applied distal force, so that the distal force can apply to the stem.

Abstract: Implant includes a body and a utile feature, for example, a smooth articulating surface. A transverse rail stem system with a plurality of rails is provided, spaced apart from the utile feature, which is adapted for transverse insertion into a bodily substrate, for example, resected bone. A surgical template—for example, to assist in sawing, drilling with a drill bit and drill guide, and broaching with a broach—along with such bone removal tools can help prepare the bone for receipt of the implant.

Abstract: A device is provided including a distal nail portion and a proximal nail portion that can be connected to each other to attain a rigid configuration. The device is to be placed internally within the medullary cavities of bones. The device is placed intramedullarily in order to minimize incision size, excessive bone resection and post-operative tendon damage and tenderness. Additionally, one particular method for using the device is provided that includes placing and affixing the distal nail in bone, placing the proximal nail in bone, connecting the distal nail to the proximal nail, doing the desired geometrical adjustments, affixing the proximal nail to the distal nail by tightening the connection and affixing the proximal nail to attain a rigid configuration.

Abstract: An intervertebral support device to impose an anatomic distance between two adjacent vertebral bodies having a pair of vertebral support elements for introduction between the edge portions of the rear half of the vertebrae, at respective substantially symmetrical positions of the instantaneous rotation axis of the natural relative flexion-extension movement of the two adjacent vertebrae. The device assists stabilizing and/or restoring the correct position of the rotation axis, which characterizes the first stage of the degenerative breakdown, without significantly limiting the relative movement of the two vertebrae. The support elements have preferably a constraint means that constrains them to the edge portions of the vertebral bodies, in particular to resist the reaction force on the intervertebral disc.

Abstract: A disc replacement device including a first body member with a convex articulation surface and a second body member with a concave articulation surface is disclosed. When operably positioned, the convex articulation surface engages the concave articulation surface to provide for movement therebetween. The disc replacement device also includes a first opening in the first body member and a second opening in the second body member, wherein the openings are angled and extends from the front aspects of the body members through the external surfaces. The disc replacement device further includes at least two bone fasteners for insertion into the first and second openings to secure the disc replacement device to a first and second vertebra. An interbody motion device and fusion implant, as well as a surgical method for implantation are also disclosed.

Abstract: An adjustable implant (10, 60, 70, 80, 90) has a base (12) and a displaceable element (16) providing opposing tissue contact surfaces (14, 18). A linkage (20, 26) is pivotally connected to the displaceable element. A linkage mover (38, 40), engaged so as to be displaceable along the base, is associated with the linkage (20, 26) so as to define a displaceable pivot location (24, 30) for pivotal motion of the linkage relative to the base, in certain preferred embodiments, the base (12) has an internally threaded track (42, 44) in which a threaded segment of the linkage mover (38, 40) is engaged, so that rotation of the threaded segment about its central axis advances the linkage mover along the threaded track, thereby displacing the displaceable pivot locations and adjusting a separation between the first contact surface and at least part of the second contact surface.

Abstract: An expandable implant device (100) for insertion between two vertebrae (400) is disclosed. The device (100) has an upper body (20), a lower body (40) and an external retainer band (60). The external retainer band (60) holds the upper body (20) and lower body (40) and has an inner surface having a plurality or set of upper ratchet teeth (80U) sloped for allowing upward movement and a plurality or set of lower ratchet teeth (80L) for allowing downward movement. The ratchet teeth (80) of the upper body (20) are mated or fitted to the upper teeth (80) of the retainer band (60) and the ratchet teeth (82) of the lower body (40) are mated or fitted to the lower ratchet teeth (82) of the retainer band (60). The height of the device (100) is increased by upward movement of the upper body (20) and downward movement of the lower body (40).

Abstract: A three column spinal fixation implant, including: an anterior cage configured to be disposed in an intervertebral space between adjacent vertebral bodies in a spine of a patient; an anterior plate coupled to the anterior cage; a pair of anterior screws coupled to the anterior cage and the anterior plate and extending posteriorly from the anterior cage and the anterior plate through a portion of one or more of the adjacent vertebral bodies and into or through posterior bony structures of the spine of the patient; a pair of anterior screws coupled to the anterior plate and extending posteriorly from the anterior plate through a portion of one or more of the adjacent vertebral bodies and into or through posterior bony structures of the spine of the patient; a plurality of posterior headbodies coupled to the anterior screws opposite the anterior cage and the anterior plate; and one or more connecting structures coupled to the plurality of posterior headbodies; wherein the three column spinal fixation implant pro

Abstract: An acetabular guide system for placing a guide pin near an acetabulum, includes a patient specific acetabular guide including an interior surface and an exterior surface, the exterior surface being configured to have a geometry to register within the acetabulum of a specific patient, a first drill insert configured to be received by the guide at a first location, the first drill insert having a first longitudinal bore configured to be received concentrically in a guide bore of the guide, the guide bore extending exterior to the interior surface, a second drill insert configured to be fixed to a boney portion exterior to the acetabulum at a second location a predetermined distance from the first location, the second drill insert forming a second longitudinal bore, and a selectively removable alignment pin configured to be received by at least one of the first longitudinal bore and the second longitudinal bore.

Abstract: An instrumented distractor includes a force sensor for measuring a force exerted by opposing surfaces of adjacent vertebrae pressing against fixed and adjustable arms on the distractor. The force on the distractor may be measured by a data acquisition system (DAS). An instrumented cage including at least one force sensor may be inserted into the same intervertebral space as the distractor and a measurement of force on the cage made by the DAS. A size and shape of the instrumented cage are preferably selected such that the magnitude of force on the cage is less than or equal to the magnitude of force measured with the distractor. In some embodiments, a first DAS is included in the instrumented distractor and a second DAS is included in the insertion handle, and the two data acquisition systems may communicate measured force values with one another.

Abstract: The present disclosure relates, according to some embodiments, to a device and/or system (e.g., redistributing weight away from a subject's foot), which may comprise (a) a platform, (b) at least one vertical support fixed to the platform and extending upwardly from the platform, and (c) at least one cuff (i) configured to surround and releasably grip at least a portion of a subject's leg other than the foot and (ii) mounted (e.g., adjustably) to the at least one vertical support at a vertical position along the at least one vertical support sufficient to suspend a subject's foot in a non-weight-bearing position above the platform during ambulation, wherein the platform, the at least one vertical support, and the at least one cuff together are configured to bear at least the subject's full weight.

Abstract: A prosthetic foot assembly is disclosed. The assembly includes a pivoting ankle joint with a hydraulic system, a prosthetic foot connected to the distal side of the ankle joint, and, at the proximal side, the ankle joint includes a transducer with pyramid adaptor for attaching to a pylon. The ankle joint sensor provides data collection during the stance and optionally, the swing, phases of walking using, for example, strain gages and accelerometers. Also disclosed are methods for real-time feature extraction. Key parameters are captured to which are applied linear, fuzzy logic, neural net, or generic algorithms to determine current state (walking flat, uphill, downhill etc.) in real time and execute changes to the angle between the ankle and foot almost instantaneously based on those parameters.

Abstract: An improved structure of a connection and adjustment assembly of a support socket joint of a prosthesis includes a connector, in which a vertical through hole and a horizontal through hole are formed. A support socket is provided on the connector and receives therein an arrest axle extending through the vertical through hole. The horizontal through hole receives therein a shaft, which has an end having a toothed wheel engageable with the arrest axle and an opposite end to which a second one-way bearing, a sleeve, and a knob cap are mounted. The knob cap has an interior that is an elliptical configuration corresponding to and mating an outside elliptical configuration of the sleeve. Pressing a knob causes movement of the sleeve and thus components mounted to the shaft so as to have the toothed wheel disengage from the arrest axle, allowing the arrest axle to be withdrawn out.

Abstract: A vacuum suspension system includes a rigid socket defining a socket wall having exterior and interior surfaces. The socket defines an aperture extending between the exterior and interior surfaces, and has a closed distal end and an open proximal end with an interior cavity defined by the interior surface. A fluid regulator is provided at the aperture and operatively engages the fluid regulator. A pump system includes a pump and a covering for securing over the exterior surface of the socket and carrying the pump. The pump is configured for placement proximate to the fluid regulator and arranged for drawing air from the socket through the aperture. A chamber having a variable volume is formed by a space defined between the exterior surface and an inner surface of the covering proximate to the pump.

Abstract: A system for delivering a surgical staple can include various components. The system may include an elongate body with a proximal end, a distal end, and a plurality of delivery platforms disposed adjacent the distal end. A sheath can move relative to the elongate body from a first position in which the distal end of the sheath is disposed distally of a distal-most distal delivery platform to a second position in which the distal end of the sheath is disposed proximally of at least one delivery platform. A plurality of intravascular tacks can be within the system with each disposed about a corresponding delivery platform.

Abstract: The present invention is directed to vascular implants and methods for fabricating the same. The implantable devices include but are not limited to stents, grafts and stent grafts. In many embodiments, the devices include one or more side branch lumens interconnected with the main lumen.

Abstract: A vascular intervention device delivery system, such as for implanting a self expanding stent, includes a thumbwheel rotatably mounted in a handle. The thumbwheel includes a radially outward thumb surface and a radially outward toothed surface that may be moved into and out of contact with a catch by mounting the thumbwheel on a pivot plate within the handle. The pivot plate may be pivoted with respect to the handle between a locked position to prevent rotation of the thumbwheel, and an unlocked position that permits rotation of the thumbwheel. A catheter has a proximal end attached to the handle, and a distal carrier segment for mounting a vascular intervention device thereon. A retractable sheath is movable from a first position covering the distal carrier segment to a second position retracted proximally uncovering the distal carrier segment. A pull extends between the thumbwheel and the retractable sheath.

Abstract: A vascular intervention device delivery system, such as for implanting a self expanding stent, includes a thumbwheel rotatably mounted in a handle. The thumbwheel includes a radially outward thumb surface. A catheter has a proximal end attached to the handle, and a distal carrier segment for mounting a vascular intervention device thereon. A retractable sheath is movable from a first position covering the distal carrier segment to a second position retracted proximally uncovering the distal carrier segment. A pull extends between the thumbwheel and the retractable sheath. A holding mechanism is operably positioned between the handle and the thumbwheel, and includes a wedge pin trapped to move in a wedge shaped cavity between a wedged position that prevents the thumb wheel from rotating, and an unwedged position that permits the thumbwheel to rotate to facilitate deployment of a self-expanding stent.

Abstract: A stent deployment system, handle, and method of loading of a medical device are provided. The system includes an outer catheter having an inner liner extending past the end of the outer catheter and an inner catheter disposed within the outer catheter. The inner liner is inverted and attached to the inner catheter. Relative movement between the outer and the inner catheters can urge the inner liner to peel away from the medical device. A handle is disposed at the proximal end of the outer catheter, and may include a splitter configured to slice the wall of the tubular member. The handle may also include a rotatable mechanism that can be attached to the tubular member. Rotation of the rotatable mechanism retracts a portion of the tubular member into the handle and winds the sliced portion about the rotatable mechanism.

Abstract: Intestinal devices and methods for facilitating weight loss. In at least one embodiment of a method of patient treatment of the present disclosure, the method comprises the step of positioning a device, that is configured to reduce or limit localized intestinal distension, around a portion of an intestine of a patient.

Abstract: The urinary bag collection cover is designed to hold and conceal the sight and smell of the drainage bag for a Foley catheter. The urinary bag collection cover is a bag featuring a drawstring closure and handle on the top of the bag that allows the bag to be hung from a hook. The urinary bag collection cover is lined with a polyethylene liner. The bottom of the urinary bag collection cover is fitted with a container within which a deodorizer is placed to mask the potential smell of urine. A port is provided in the urinary bag collection cover to allow for the insertion of a drainage tube to draw off the urine collected in the urinary bag collection. The urinary bag collection cover comprises a bag, a handle, a drawstring, a drainage port, and a deodorizer container.

Abstract: A device and a method for creating and/or maintaining an obstruction free upper respiratory passages. The device is configured to fit under the chin of a subject adjacent to the subject's neck at an external location corresponding approximately with the subject's internal soft tissue associated with the neck's anterior triangle. The device is capable of exerting negative pressure on the surface of a subject's neck, displacing the soft tissue forward and enlarging the airway.

Abstract: Disclosed herein are mandibular advancement devices comprising an upper splint and a lower splint, where the upper splint comprises one or more upper fins, where each upper fin is located at a distance UD from back of the upper splint; the lower splints comprise one or more lower fins, where each lower fin is located at a distance LD from back of the lower splint; where the position of the upper and lower fins is unchangeable. Also disclosed are methods of reducing partial constriction of airway during sleep for a patient, the method comprising identifying a patient in need thereof; and administering to the patient the disclosed mandibular advancement device. Also disclosed are methods of manufacturing a mandibular advancement device, the method comprising obtaining measurements from a patient's dentition; digitally designing a mandibular advancement device; and milling the mandibular advancement device.

Abstract: A method and delivery system are disclosed for creating an aqueous flow pathway in the trabecular meshwork, juxtacanalicular trabecular meshwork and Schlemm's canal of an eye for reducing elevated intraocular pressure. Pulsed laser radiation is delivered from the distal end of a fiber-optic probe sufficient to cause photoablation of selected portions of the trabecular meshwork, the juxtacanalicular trabecular meshwork and an inner wall of Schlemm's canal in the target site. The fiber-optic probe may be advanced so as to create an aperture in the inner wall of Schlemm's canal in which fluid from the anterior chamber of the eye flows. The method and delivery system may further be used on any tissue types in the body.

Abstract: A device for delivering a treatment medium to an eye includes a first body portion configured to be removably inserted and secured in an opening of the eye, and a second body portion supported by the first body portion. At least the second body portion includes a treatment medium, and a coating having an opening through which the treatment medium elutes out of the device.

Abstract: A dual blade device and method useable for performing an ab interno procedure within a human eye to remove a strip of trabecular meshwork tissue.

Abstract: Laser assisted cataract surgery methods and devices utilizing one or more treatment laser beams to create a shaped opening in the anterior lens capsule of the eye when performing a capsulorrhexis procedure. A light absorbing agent may optionally be added onto or into the lens capsule tissue, and the treatment laser wavelength selected to be strongly absorbed by the light absorbing agent. Alternatively, the treatment laser wavelength may be selected to be absorbed or strongly absorbed by the tissue itself, in which case no additional light absorbing agent need be used. Visualization patterns produced with one or more target laser beams may be projected onto the lens capsule tissue to aid in the procedure. The devices may be attached to or integrated with microscopes.

Abstract: A surgical system includes a laser source to generate a first set of laser pulses; a guiding optic to guide the first set of laser pulses to a target region; a laser controller to generate an electronic representation of a target scan pattern, and to control the guiding optic to scan the first set of laser pulses according to a portion of the target scan pattern to create a first photo-disrupted region in the target region; and a OCT imaging system to generate an image of a portion of the first photo-disrupted region. The laser controller can generate an electronic representation of a modified scan pattern in relation to the image generated by the SS-OCT imaging system, and control the guiding optic to scan a second set of laser pulses according the modified scan pattern.

Abstract: Embodiments disclosed within herein relate to a wound dressing, suitable for use in negative pressure wound therapy, comprising a body of porous material, the body of porous material comprising a plurality of cuts which provide regions of flexibility within the body. Further embodiments relate to methods of manufacturing and method of use of such wound dressings. In addition, the wound dressing can comprise a retaining mechanism removably coupled to the material and configured to retain the material in the expanded conformation.

Abstract: A method for manufacturing absorbent articles comprises delivering a continuous web assembly including a backsheet material, a liquid permeable bodyside liner material, and an absorbent structure interposed between the backsheet material and the bodyside liner material, the web assembly having a body-facing side and a garment-facing side; attaching a discrete segment of first waist elastic material to the body-facing side of the web assembly; attaching a discrete segment of second waist elastic material to the garment-facing side of the web assembly such that the web assembly is interposed between the discrete segments of first and second waist elastic materials; and cutting the web assembly to form a plurality of absorbent articles.

Abstract: Provided is a tampon applicator having one or more insertion indicators to gauge and/or control the insertion depth of a tampon. The one or more insertion indicators may be located on the tampon applicator barrel, plunger, tampon, removal string, or any combinations thereof. As a result of the one or more insertion indicators, a woman can adjust the insertion depth of the tampon to her body's requirements ensuring leakage protection, comfort, or both.

Abstract: A sensor for detecting urine and stool secretion mounted over two or more layers of garment, said sensor comprising: at least one light source configured to illuminate said garment; at least one photodetector configured to output an indication of the amount of light reflected from said garment; and an electronic circuit configured to detect said secretion by monitoring said output of said photodetector and identifying a temporal pattern being characteristic of said secretion event.

Abstract: A packaged feminine care absorbent article has an absorbent article with an absorbent structure and a shell. The absorbent structure is configured for disposition adjacent a female wearer's vaginal region. The shell is configured for supporting the absorbent structure at the vaginal region. The shell has a body-facing surface and a garment-facing surface. The body-facing surface has an adhesive thereon for adhering the shell directly to the wearer. The absorbent structure is attached directly to the garment-facing surface. The absorbent article is configurable between a packaged configuration and a use configuration. The absorbent structure is folded longitudinally about at least one transverse fold line and transversely about at least one longitudinal fold line in the packaged configuration. A portion of the shell overlies a portion of the absorbent structure in the packaged configuration.

Abstract: A multi layered sanitary pad having a unique shape and design for snug fit, increased absorption, comfort, obscurity and enhanced leak prevention that includes a body made up of embossed fleece layers. The upper surface of the sanitary pad includes a central protrusion extending longitudinally and laterally from end to end and side to side, the cross-shaped protrusion including additional cotton wadding, for increased absorption and leak prevention for extended wear. The top surface protrusion is shaped and sized to slightly penetrate the vaginal opening to ensure a snug comfortable fit to increase absorption and enhance leakage prevention along with extended wear. The top surface includes (4) recessed portions surrounding the central protrusion area, for a snug fit, additional absorption, leakage prevention and comfort.

Abstract: An absorbent article comprising a first and second plurality of elastics. The first plurality of elastics may be disposed in a front and a crotch region. The second plurality of elastics may be disposed in a back region and the crotch region. The first and second plurality of elastics may be linear and parallel with a transverse axis of the article.

Abstract: A diaper structure with enhanced softness attributes is disclosed. The diaper structure may include an innermost layer formed of a first nonwoven web, and an outermost layer formed of a second nonwoven web. The first and second nonwoven webs may have a combined basis weight of at least about 30 gsm. The ratio of the first web basis weight to the second web basis weight may range from 30/70 to 70/30.

Abstract: A disposable diaper having front and rear augmented waistband zones having a specified size and stiffness is disclosed. For relatively thinner, less bulky diapers of currently marketed designs, providing augmented waistband zones is believed to reduce mental and physical effort for the caregiver in application of the diaper. The augmented waistband zones provide a robust-feeling structure proximate the waist edges, which the caregiver may grasp at front and rear to adjust the diaper on the wearer. Caregiver perception of a need to reach deeper into the diaper structure to grasp it at a thicker area to tug at it is believed to be reduced.

Abstract: A composite liquid-retentive substrate for a hygiene article comprises a base layer of first liquid-absorptive material. The base layer having a posterior end and a diametrically opposed anterior end interconnected by an intermediate tapered region. The posterior end has opposing posterior corners and the anterior end has opposing anterior corners. A posterior liquid-flow abutment comprising second absorptive material is disposed substantially around a perimeter of the posterior end. At least one anterior liquid-flow abutment comprising second absorptive material is disposed proximate one of the anterior corners of the anterior end.

Abstract: A bandage pulling tool has a thin elongate body and a hole extending transverse to a longitudinal axis of the thin elongate body proximate an end thereof. In use, a first end of a bandage is secured to the tool using the hole by passing a first end of the bandage through the hole for use as an anchor point to the tool. With the bandage thus secured to the tool in a position passing through the hole therein, the first end of the bandage can be passed from a first side of a body portion of an injured party to another behind the body portion using the elongated shape of the tool. Accordingly, a wrap around bandage can be applied to the patient with minimal, if any, movement of potentially injured areas compared to prior art techniques of manually feeding the bandage behind the injured party.

Abstract: A method is disclosed for deploying a ramp assembly. The ramp assembly includes a ramp portion rotatable between a stowed position and a deployed position. The ramp assembly further includes a panel rotatable about a first end, wherein the ramp portion supportingly engages a second end of the panel to elevate the second end of the panel as the ramp portion moves toward the deployed position. The method includes the step of rotating the ramp portion until the ramp portion contacts an alighting surface. The method further includes the step of rotating the ramp portion until one of a first condition and second condition occurs. The first condition is that the ramp portion has reached a maximum slope. The second condition is that the second end of the panel has reached a predetermined elevation.

Abstract: A device for securing a mobility device in a mobility vehicle or on a lifting device that is installed in or on a mobility vehicle or trailer.

Abstract: A patient assistance and rehabilitation device or more specifically a patient mechanical lift device that can be utilized as patient walker, a seat, a seated transporter, a toilet, a table and a rehabilitation device. The patient assistance and rehabilitation device including a power band or tension motor to help a patient move from a sitting to a standing position and to supplement an exercise or rehabilitation program.

Abstract: A system for use with a bed having a frame and a supporting surface includes a sheet having a bottom surface placed above the supporting surface of the bed, a top surface, and a plurality of tether straps connected to and extending from the sheet. Each tether strap is configured for connection to the bed. The bottom surface is at least partially formed of a low friction material, and the top surface is at least partially formed of a high friction material, such that the top surface provides greater slipping resistance than the bottom surface. The tether straps include at least two pairs of tether straps, with one pair connected proximate a top edge of the sheet and another pair connected proximate a bottom edge of the sheet. The sheet may further include a sliding member on the bottom surface to assist in lateral sliding of the sheet.