Abstract: Marking device (100) for implantation into a tissue (260), having a support structure (102) which is formed by at least one elastic metal wire, is compressible and is self-expanding and which, in an expanded state, encompasses an interior space (104), characterized in that the marking device (100) is designed to transform itself on its own from a compressed state into an expanded state, even against a tissue pressure prevailing at a tissue site to be marked, and the marking device (100) in the expanded state has a hollow, approximately spherical shape.

Abstract: A head-worn image display apparatus that comprises a non-immersive image display assembly that receives images from a stereoscopic video camera module. The image display assembly comprises a miniature display component for generating the images for display. The image display assembly may work by an optical relay system. The head-worn image display apparatus could be used in a variety of different settings. One particular application is for performing medical procedures such as microsurgery. The stereoscopic video camera module may have optical magnification capability (e.g. such as in a surgical microscope) to provide a magnified view of the surgical field.

Abstract: A device for surgical assistance is disclosed. The device comprising one or more rails, and a plurality of side posts. The rails are configured to attach to a hand table via one or more engagement members. The plurality of the side post comprises an upper part and a lower part. The lower part of the said side post is engaged to the rails via a clamp mechanism. The upper part of the said side post is configured to hold surgical equipment. Further, each of the side post is height adjustable. The device further comprises a rail extension system, which is attached to an end portion of rails lying close to a trunk portion of the patient.

Abstract: The present invention relates to a surgical dental tool for assisting with the implantation of a dental implant. The tool is designed to create an opening in a patient's jaw into which the dental implant will be inserted. In one embodiment, the tool includes a handle, a blade carrier, a pick and a blade stabilizing channel formed in at least a portion of the blade carrier and extends through at least a portion of the pick. The blade stabilizing channel receives and stabilizes a cutting blade. The blade carrier may include an adjustable clamping plate for removably securing the cutting blade in the blade stabilizing channel. The pick may include a sheath that receives and protects the tip of the cutting blade from breakage when the blade is in the blade stabilizing channel and is being used to cut a dental implant opening.

Abstract: An absorbent insert of compressed matrix of absorbent material, including a filler dispersed therein to improve stiffness/rigidity of the insert and controls the absorbency of the compressed absorbent material. The insert is pre-shaped and sized for inserting into a tooth cavity, such as a pulp chamber or a root canal space. The compressed insert expands or swells upon absorbing fluid within the tooth cavity, so as to more completely dry the tooth cavity. The absorbent insert also serve as a substrate of an applicator for medical agent to be applied to a tooth cavity. The absorbent insert is provided (e.g., coated or impregnated) with a medical agent, which medical agent is released into the tooth cavity as the absorbent material absorbs fluid in the tooth cavity.

Abstract: A matrix adapted is for the specific tooth type, and is positioned on the tooth to covers the tooth, so that an injected curable material is encased by the matrix over the tooth. When the curable material has cured, the matrix is removed, resulting in a veneer on the tooth.

Abstract: An orthodontic space closure device is provided, including a first tooth cap unit, a second tooth cap unit, and a number of elastic members. The first tooth cap unit is configured to be removably worn on the anterior teeth of a dental arch of a patient. At least one first connector is fixed on each buccal side of the first tooth cap unit. The second tooth cap unit is configured to be removably worn on the posterior teeth of the dental arch. A vertical extension part is formed on each buccal side of the second tooth cap unit, and at least one second connector is fixed on each vertical extension part. The elastic members couple the first connectors to the second connectors, thereby exerting elastic traction forces having horizontal and vertical components on the first tooth cap unit to achieve retraction and intrusion of the anterior teeth.

Abstract: A dental tools system with a plurality of guide tabs; a mold and a plurality of tissue punch heads. The mold has a plurality of mold holes, each mold hole having a top portion and a bottom portion. Each guide tab fits in the top portion of one of the mold holes and each tissue punch head fits in the top portion of one of the mold holes. A method of placing dental implants is also described.

Abstract: A method of placing a dental implant without the use of traditional tools such as a mallet or an electric drill to create the opening in the patient's jaw bone that will receive the dental implant is provided. This method may include the steps of creating an implant opening, incising the opening, refining the opening and inserting the dental implant in the opening. A piercing instrument may be used to create the opening, a first cutting tool may be used to incise the opening, a second cutting tool may be used to refine the opening and a hand operated driver may be used to insert the dental implant into the opening. In at least one embodiment, only a hand force is applied to the instruments used to carry out the method without the use additional instruments to create or augment the force being applied to the instruments being used.

Abstract: A dental tool for resurfacing thread forms of a dental implant is disclosed. The tool includes a main body having a cylindrical member with a slot. A blade having a head is inserted in the slot to orient the head to protrude from the interior surface of the cylindrical member of the main body. The main body may be rotated into traversing a thread form of the implant. A compression sleeve is inserted over the main body. The compression sleeve has an open position and a closed position to hold the blade in the slot. The compression sleeve may be flexed by relative movement of the blades to resurface threads of a tapered dental implant.

Abstract: A method for determining and drawing the ideal individual shape of the two front upper teeth uses at least one image of the patient's face in front view, non-smiling and with the mouth closed, and at least one image of the patient's face in front view, smiling and with closed teeth.

Abstract: The invention relates to a coloured curable composition for use in an additive manufacturing process, the composition comprising a curable resin composition comprising radiation curable components, a photo initiator, a dye composition comprising a dye D1 and a dye D2, dye D1 having a light absorption maximum within a wave length range from 400 to 530 nm, dye D2 showing a light absorption maximum within a wave length range from 540 to 650 nm. The invention also relates to a 3-dim composite article obtained by processing the curable composition in an additive manufacturing process.

Abstract: The present invention discloses occlusal locks and positioning handles as part of an upper and/or lower denture or other prosthetic solution, the locks facilitating alignment construction and delivery of the conversion prosthesis, expediting the clinical procedure, and ensuring accurate alignment that improves the accuracy of rapid tooth replacement procedures.

Abstract: A damping dental post key configured to implant a dental root post for restoration of a tooth is described. The dental post key includes a body for handling and a post carrier having a key shape with respect to a head portion of the dental root post. During implantation of the dental post, rotation of the body compresses a set of springs in contact with the post carrier reducing a reaction force to a tooth root. In this way a limited force will be applied and a root fracture can be prevented. Further, the dental post key can be configured to have a fixed movement in a counterclockwise direction to remove the dental post and a free quarter-cycle movement with effort in a clockwise direction.

Abstract: A bite rim system includes a plurality of dental bite rims having a shape and size that is suitable for use in a human mouth. A plurality of anatomically correct replica teeth are provided that include various tooth characteristics of different shapes, thicknesses, sizes and colors. A series of replica teeth are removably pre-mounted onto one or more of the bite rims in an anatomically correct pattern. The system also includes one or more replica teeth strips having a front facing surface with the image of one or more teeth imprinted thereon, and a back facing surface that is coated with an adhesive material for mating with one of the dental bite rims.

Abstract: An oral irrigator contains: a body, a water tank and a detachable jet tip which are both in connection with the body, a power device and a control device Which are both accommodated in the body. The power device is configured to deliver water from the water tank to the detachable jet tip. The power device includes a first outlet defined thereon and configured to discharge the water, a delivery tube connecting with the first outlet, and a first seal element configured to stop water flowing into the body from the power device so that the water discharges out of the first outlet.

Abstract: A curing light assembly includes a housing, a base for supporting the housing in a storage position, a light source supported by the housing, and a controller configured to operate the light source. The light assembly further includes a light sensor in communication with the controller, which light sensor is operable to detect light emitted from the light source when the housing is supported in the storage position, and with the controller configured to calibrate the light source based on light detected by the light sensor from the light source when the housing is supported in the storage position.

Abstract: A case for a dental treatment device includes a bottom panel having an inner surface and an outer surface. The inner surface of the bottom panel defines a first concave portion that corresponds to a shape of a bottom of the dental treatment device. The first concave portion forms a corresponding first convex portion of the outer surface of the bottom panel. The case also includes a top panel having an inner surface and an outer surface. The inner surface of the top panel defines a second concave portion that corresponds to a shape of a top of the dental treatment device. The second convex portion forms a corresponding second convex portion of the outer surface of the top panel.

Abstract: A surgical procedure kit for inserting a medical tube according to the present invention includes: an insertion pathway formation means configured to include a medical tube provided with a hollow tube main body, a tube member including a hollow conduit having the medical tube received therein and forming a pathway into which the medical tube is to be inserted, and a support member including a support rod which is inserted into the medical tube and has stiffness greater than that of the tube member; and a push means configured to be slidable within the conduit of the tube member and push the medical tube through the conduit of the tube member.

Abstract: Devices and methods for treating an abdominal incision or hernia are described. An implant for the restoration or prophylactic treatment of an abdominal wall comprises an elongate element and at least one sheet connected to the elongate element along a longitudinal axis of the elongate element. The elongate element is positioned along the line of incision, and the at least one sheet is secured to the abdominal muscles surrounding the incision.

Abstract: A rapid exchange catheter having a vena cava filter and a method for percutaneous delivery of the rapid exchange vena cava filter for use in indicated medical situations in which prophylactic or therapeutic protection against pulmonary embolism are indicated.

Abstract: An implantable device consisting of a plurality of links and configured to be in one of two modes, either flexible in at least one plane or rigid in all planes. The implantable device is inserted into a body cavity in the flexible mode and transformed to the rigid mode resembling a figure eight and anchoring the device in the body cavity.

Abstract: A method of using an implantable device provides an implantable device including a plurality of links (113, 115, 117, 119), a device closure pin (111), a lock-in unit (103) attached and located between two links, and a quick release unit (105) attached and located between two links. The plurality of links (113, 115, 117, 119), lock-in unit (103) and release unit (105) are constructed in a closed contour. The closed contour of the implantable device, in a rigid state (151), is a figure eight comprised of two arcs (125, 127) and two connected interconnecting sections (131, 133).

Abstract: A method and apparatus for attaching tissue to bone in a shifted position without requiring surgical detachment of muscle or connective tissue joining the tissue layer to the bone layer. The skin and/or soft tissue layer is displaced in a surgical or non-surgical manner and a fastener of the invention is driven through the skin and/or soft tissue layer into the periosteum or bone layer to affect a tissue repositioning procedure. The method and apparatus may also be used to attach tissue to tissue an a shifted position.

Abstract: A device for attaching soft tissue to a prosthetic implant. The device includes a body that includes a frame and a porous section disposed within the frame, wherein the porous section permits the passage of body fluids therethrough to encourage the healing of the soft tissue as well as the growth of soft tissue into and through the porous section.

Abstract: An adjustable construct for fixation of a tendon or ligament graft in a tunnel. The construct comprises a flexible, adjustable loop connected to tissue (for example, graft, ligament or tendon). The adjustable loop may be integrated with an additional tissue supporting device (for example, a wedge or a plug). The tissue is secured within a bone socket/tunnel by adjusting the length of the flexible adjustable loop.

Abstract: A ligament assembly comprising a first ligament anchor (9) connected to a second ligament anchor (14) by a ligament (18) a resilient element (40) being associated with the first ligament anchor (9) and a ligament tension adjuster (44, 50) being associated with the second ligament anchor (14). The resilient element (40) may be disposed within the first ligament anchor (9) and the ligament tension adjuster (44, 50) may be disposed within the second ligament anchor (14).

Abstract: An ophthalmological implant includes a main structure with a central aperture, a first side, and a second side arranged opposite the first side. It further includes a plurality of pigment arrangements arranged in the main structure, at least one of the pigment arrangements includes at least one color pigment and an enclosure that encloses at least most of the at least one color pigment.

Abstract: An ophthalmic visualization system includes a rear illumination system, to generate and to project a rear illumination light onto a retina of an eye that has an intraocular lens (IOL) implanted into the eye, so that the rear illumination light reflects from the retina as a reflected illumination light, wherein a central portion of the reflected illumination light propagates through the IOL to form an IOL-focused illumination light, and a peripheral portion of the reflected illumination light propagates around the IOL to form a peripheral illumination light; an optic, to receive the IOL-focused illumination light and the peripheral illumination light from the eye, and to transmit the received illumination lights; an aperture slop, to stop the transmitted peripheral illumination light, and to allow the IOL-focused illumination light to pass through; and an imaging system, to form an isolated IOL image based on the transmitted IOL-focused illumination light.

Abstract: A middle ear prosthesis is made of a stiff deformable material and includes a planar head end with a central portion having a central diameter. The head end is adapted for engagement with a tympanic membrane from the middle ear of an implanted patient. An opposing pair of U-shaped stapes engagement legs bend down from the central portion so that an end distance between ends of the engagement legs is less than the central diameter. The engagement legs are adapted for adjustable length engagement with the stapes in the middle ear of the implanted patient. The head end and the engagement legs are adapted to transmit vibrations from the tympanic membrane to the stapes for perception as sound by the implanted patient.

Abstract: An occluder device for occluding a gap between a medical device and adjacent body tissue includes a conformable body having a hollow interior, a leading end and a trailing end; and a port disposed at the trailing end of the body and in fluid communication with the interior of the body.

Abstract: A heart valve repair device, comprising an atrial-fixation member having an expandable mesh configured to have oval or circular shape in a deployed configuration, the atrial-fixation member defining a central lumen; and a baffle extending from a portion of the atrial-fixation member, the baffle having an anterior portion with a smooth, atraumatic surface configured to coapt with at least a portion of one or more native leaflets of a native heart valve, a posterior portion configured to engage and displace at least a portion of another native leaflet of the native heart valve, wherein the baffle extends radially inward from the atrial-fixation member into the central lumen to approximate a closed position of the displaced native leaflet.

Abstract: An expandable and collapsible stent comprising prosthetic leaflets attached to an inner valve support section that extends radially upward into an outer stent section. A transition stent section is disposed between the inner valve support section and the outer stent section. Each of the outer stent section, the inner valve support section and the transition stent section may comprise struts or the equivalent that form and define cells having a pattern, wherein each section may comprise a different cell pattern. Transition stent section preferably comprises struts that are of equal curvature, with adjacent struts equally spaced from each other to allow nested collapsing of the transition stent section struts. A boss section extending downstream away from the inner valve support section may be provided to aid in alignment and retention of the expanded stent and may comprise a shape that is complementary to a heart chamber annulus.

Abstract: A stent-valve for transcatheter implantation to replace a cardiac valve, the stent valve being compressible to a compressed state for delivery, and expandable to an operative state for implantation, the stent-valve comprising a stent, a plurality of leaflets for defining a prosthetic valve, an inner skirt, an outer skirt, and a paravalve seal for sealing against surrounding tissue. In some embodiments, the paravalve seal comprises material that swells in response to contact with blood. In some embodiments, the seal comprises a flap or pocket that is distensible in response to backpressure and/or paravalve back-flow of blood.

Abstract: A method of assembling a prosthetic heart valve includes providing a collapsible and expandable stent having an annulus section and an aortic section. The annulus section has a first diameter in a relaxed condition and a second diameter less than the first diameter in a collapsed condition. A constraint is applied to the stent to constrain the annulus section to a predetermined diameter between the first and second diameters. Applying a cuff and/or a plurality of leaflets to the stent in the constrained condition enables less material to be used. The resultant prosthetic valve is therefore able to be collapsed to a smaller diameter for introduction into a patient.

Abstract: A two-stage or component-based valve prosthesis that can be quickly and easily implanted during a surgical procedure is provided. The prosthetic valve comprises a support structure that is deployed at a treatment site. The prosthetic valve further comprises a valve member configured to be quickly connected to the support structure. The support structure may take the form of a stent that is expanded at the site of a native valve. If desired, the native leaflets may remain and the stent may be used to hold the native valve open. In this case, the stent may be balloon expandable and configured to resist the powerful recoil force of the native leaflets. The support structure is provided with a coupling means for attachment to the valve member, thereby fixing the position of the valve member in the body. The valve member may be a non-expandable type, or may be expandable from a compressed state to an expanded state.

Abstract: A method of delivering a prosthetic mitral valve includes delivering a distal anchor from a delivery sheath such that the distal anchor self-expands inside a first heart chamber on a first side of the mitral valve annulus, pulling proximally on the distal anchor such that the distal anchor self-aligns within the mitral valve annulus and the distal anchor rests against tissue of the ventricular heart chamber, and delivering a proximal anchor from the delivery sheath to a second heart chamber on a second side of the mitral valve annulus such that the proximal anchor self-expands and moves towards the distal anchor to rest against tissue of the second heart chamber. The self-expansion of the proximal anchor captures tissue of the mitral valve annulus therebetween.

Abstract: Systems, devices and methods for resizing a valve annulus are described. An implant is delivered proximate a mitral valve, the implant comprising a tubular body and a plurality of piercing helical anchors, the tubular body comprising an proximal diameter and a distal diameter. Tissue proximate the mitral valve is engaged by rotating the plurality of anchors with corresponding rotational drivers. The tubular body may be transitioned from a first structural configuration having the proximal diameter smaller than the distal diameter to a second structural configuration having the proximal diameter larger than the distal diameter.

Abstract: A cord that has been previously affixed around an annulus can be fastened using a sliding member that locks into a housing. Before those two parts are locked together, the cord is free to slide through a channel in the sliding member, and a shear pin prevents the sliding member from moving. After those two parts are locked together, portions of the cord are squeezed between the upper surface of the sliding member and one wall of the housing, and other portions of the cord are squeezed between the lower surface of the sliding member and another wall of the housing, so that the cord can no longer slide. After locking, a sliding cutting element can be actuated to cut off portions of the cord that are proximal with respect to the two locked parts.

Abstract: A cord that has been previously affixed around an annulus can be fastened with a fastener that is movable from a first state in which the cord is free to slide to a second state in which the cord is locked in place. After the fastener is moved to the second state, a cutting element with a slit shaped distal portion oriented in the distal-to-proximal direction with sharp edges slides with respect to a shelf and cuts off portions of the cord that are proximal with respect to the two locked parts.

Abstract: A method and device for anchoring a prosthetic heart valve or annuloplasty ring to a valve annulus in a heart and a method of implanting same is disclosed. The device can include a prosthetic valve or annuloplasty ring with one or more anchors configured to be threaded or otherwise passed underneath a native leaflet and/or subvalvular tissue to secure the device at the native annulus.

Abstract: A delivery system and method for delivery of an annuloplasty implant for a patient are disclosed. The delivery system comprises a commissure locator device for locating a commissure, comprising; an extension member, a catheter, and wherein the extension member is extendable relative the catheter for location of at least one commissure of a cardiac valve, and a coronary sinus contractor for temporary insertion into the coronary sinus (CS) and having a displacement unit being temporarily transferable to an activated state in Which the shape of the annulus Of the heart valve is modified to a modified shape to be retained by said annuloplasty implant.

Abstract: A device for measuring heart valve for sizing a heart valve reinforcement ring, includes a first handle having a first shaft an outer ring coupled to the first shaft, wherein the outer ring has an inner surface; and an inner ring having an outer surface, wherein the inner ring is removably couplable to the outer ring. The inner surface of the outer ring and the outer surface of the inner ring further have reciprocal mating surfaces configured and arranged to grip sutures therebetween when coupled together. The device may further have a second handle with a second shaft connected to the inner ring. Alternatively, the first handle may have a second shaft that is connected to a second outer ring.

Abstract: A cartilage repair implant, an auxiliary surgical tool kit and a cartilage repair system are provided. The cartilage repair implant includes a body and a plurality of pins. The body is a porous structure and is configured to carry cartilage repair material. The pins are fixed to the body for being inserted into a patient's bone. The auxiliary surgical tool kit includes a positioning sleeve and a click tool. The positioning sleeve has a through passage. A first alignment structure is disposed on the sidewall of the through passage. The click tool includes an outer tube and a push rod. A second alignment structure mutually aligned with the first alignment structure is disposed on the outer wall of the outer tube. The outer tube is configured to pass through the through passage. The push rod is slidably disposed in the outer tube. One end of the outer tube has a shaping blade for slicing a to-be-implanted region on an affected area of the patient.

Abstract: This invention relates to and orthopaedic implant having an expansion means adapted to increase the external surface area of the implant, the expansion means positioned to correspond to voids or depressions in the anatomy of a patient. Also described are method for the design and manufacture of such implants.

Abstract: Systems, devices, and methods for providing orthopedic implants that reduce the negative effects of stress shielding on surrounding bone structure. The orthopedic implants include two portions, a shell portion that forms an articulation interfaces and an intermediate portion that forms a bone interface. The shell portion is designed to reduce absorption of Carticulation forces and evenly distribute incident forces to the intermediate portion. The intermediate portion is designed to form a strong interface with native bone and transmit forces from the shell into the bone.

Abstract: A glenoid implant that is 3D-printed or machined from ceramic and/or metal as a substitute for an autograft or allograft in a surgical repair. Structural supports composed of metal are designed in the interior of the implant for support during implantation and post-operation. The remainder of the volume of the implant is composed of a material having optimal pore structure for rapid bone integration and healing.

Abstract: Provided is single, monolithic wrist implant for the proximal carpal row.

Abstract: An intervertebral implant includes a core member operably coupled between an upper and a lower base member. An outer cavity extends between the core member upper end and lower end, and radially between the inner cavity and an outer surface of the core member. A core member inner wall is formed between the inner and an outer cavity, and a core member outer wall is formed between the outer cavity and the outer surface of the core member. A first locking member is positioned on at least one of the core member upper end and the core member lower end and at least one second locking member is positioned on an inner surface of at least one of the upper and lower base member for locking engagement. The upper and lower end of the core member are oriented at a lordotic angle ranging from 1 degrees to 20 degrees.

Abstract: An expandable spinal implant includes a distal projection extending from only one side of the implant, ending in an anterior tip, the anterior portion and anterior tip defining an elongated distal end hook, which is wider than the proximal end. The distal end hook rotates around the spinal cord, aligning the implant with a desired pathway, then inserts into place in the disc space between the vertebrae. The elongated widened distal end hook provides a TLIF approach, distributes loads, provides anterior rim engagement, and creates lordosis.