Abstract: Described herein are shock wave devices and methods for the treatment of calcified heart valves. One variation of a shock wave device may comprise an elongated flexible tube carried by a sheath. The tube may have a fluid input end, which may be located near a proximal end of the sheath. The tube may include a loop portion. The loop portion may be configured to be at least partially accommodated within a cusp of the heart valve. The tube may be fillable with a conductive fluid. In some variations, the shock wave device may include an array of electrode pairs associated with a plurality of wires positioned within the loop portion of a tube. The electrode pairs may be electrically connectable to a voltage source and configured to generate shock waves in the conductive fluid in response to voltage pulses.

Abstract: An end effector apparatus for a surgical instrument is disclosed. The apparatus includes a first jaw mounted on a first revolute joint, the first jaw having a manipulating portion extending forwardly from the first revolute joint and a lever arm projecting rearwardly from the first revolute joint. The apparatus also includes a second jaw having a manipulating portion generally opposing the manipulating portion of the first jaw, and a coupler having an actuation end disposed overlapping the lever arm of the first jaw, the first and second jaws being laterally spaced apart to provide clearance for the actuation end of the coupler. The apparatus further includes a linkage extending rearwardly between the actuation end of the coupler and the lever arm of the first jaw, the linkage being operable to cause opening and closing movements of the first jaw about the first revolute joint in response to reciprocating movement of the coupler.

Abstract: An endoscopic surgical blade is disclosed. The blade is of a low-profile design, having a downward angled cutting surface that is radiused at its upper end. The blade is part of an endoscopic knife assembly which also contains a knife tube. The endoscopic knife assembly is for use in endoscopic surgery by insertion of the assembly through a slotted cannula. The knife tube is hollow and allows the insertion of an endoscope for viewing of the surgical procedure. A method for a performing an operative procedure on a target tissue in a subject using an endoscopic knife assembly having a low-profile, downward angled blade is also described.

Abstract: An example thrombectomy device is disclosed. The example thrombectomy catheter includes a catheter tube including a proximal portion, a distal portion and a lumen extending therein. The thrombectomy catheter also includes a high pressure tube extending through the catheter lumen from the catheter proximal portion toward the catheter distal portion, the high pressure tube having at least one jet orifice for directing at least one fluid jet through the catheter lumen. The thrombectomy catheter also includes an outflow orifice, an inflow orifice and a fluid pulse generator coupled to the proximal portion of the catheter tube, wherein the fluid pulse generator is configured to inject fluid though the thrombectomy catheter at a first frequency.

Abstract: A method and device for perforating an aortic valve to remove excessive calcium deposits on aortic valve leaflets improves the implantation of TAVI replacement valves in patients. By removing excessive calcium deposits, the radial pressure exerted by implanted TAVI replacement valves is reduced, such that there is less blood leakage around the valve and less stress on the cardiac conductive system. A device with a collapsible punch is inserted into the aortic valve. The punch is separable such that the aortic valve leaflets are positioned between at least two elements of the punch. The two elements then compress together with the leaflets between them, causing the aortic valve to be perforated. A circumferential ring of the remaining aortic valve and calcium deposits are left to provide stability for the TAVI replacement valve.

Abstract: A treatment method is a treatment method for cutting cartilage of a human body by an ultrasonic device including a cutting section that ultrasonically vibrates. The treatment method includes cutting the cartilage with a product of an amplitude of the cutting section and a pressing force for pressing the cutting section against the cartilage being 100 (N·?m) or larger.

Abstract: In one embodiment, a surgical instrument comprises an articulable waveguide. The articulable waveguide may be configured to transmit ultrasonic energy therealong. The articulable waveguide comprises a proximal drive section, an end effector and a first flexible. The proximal drive section is configured to couple to an ultrasonic transducer. The end effector is located at a distal portion of the articulable waveguide. The first flexible section comprises a flex bias and be positioned between the proximal drive section and the end effector. The surgical instrument further comprises a first tine extending longitudinally relative to the articulable waveguide.

Abstract: An apparatus for locating and accessing an epidural space within a patient. The apparatus includes a handle having a top end and a bottom end. A handle channel is formed through the handle running from the top end to the bottom end. A proximal end of a hollow needle extends from the bottom end of the handle and aligns with the handle channel. A distal end of the hollow needle is sharp and pointed. An obturator is disposed within the hollow needle and the handle channel. A distal end of the obturator is rounded and blunt and extends from the distal end of the hollow needle. A proximal end of the obturator extends beyond the handle channel at the top end of the handle.

Abstract: Disclosed herein is a lifting surgical instrument having a branch point, which is used to insert a thread without a cog and a barb into the skin. The lifting surgical instrument includes a sheath, including: a probe part formed in the tubular shape in which a through hole penetrating in a longitudinal direction is formed, and configured such that the front end thereof may be inserted into the skin; and a body M configured to extend from the rear end of the probe part, to have a diameter larger than that of the through hole, to communicate with the through hole, and to include a sheath hole. In this case, a direction guidance portion is provided on the inner surface of the probe part, and the angle at which the needle travels is changed via the direction guidance portion when the needle passes through the through hole.

Abstract: Surgical access port stabilization systems and methods are described herein. Such systems and methods can be employed to provide ipsilateral stabilization of a surgical access port, e.g., during spinal surgeries. In one embodiment, a surgical system can include an access port configured for percutaneous insertion into a patient to define a channel to a surgical site and an anchor configured for insertion into the patient's bone. Further, the access port can be coupled to the anchor such that a longitudinal axis of the access port and a longitudinal axis of the anchor are non-coaxial. With such a system, a surgeon or other user can access a surgical site through the access port without the need for external or other stabilization of the access port, but can instead position the access port relative to an anchor already placed in the patient's body.

Abstract: Adjustable-length surgical access devices are disclosed herein, which can advantageously allow an overall length of the access device to be quickly and easily changed by the user. The access devices herein can reduce or eliminate the need to maintain an inventory of many different length access devices. In some embodiments, the length of the access device can be adjusted while the access device is inserted into the patient. This can reduce or eliminate the need to swap in and out several different access devices before arriving at an optimal length access device. This can also reduce or eliminate the need to change the access device that is inserted into a patient as the depth at which a surgical step is performed changes over the course of a procedure. Rather, the length of the access device can be adjusted in situ and on-the-fly as needed or desired to accommodate different surgical depths.

Abstract: A device to protect the perineal and an extraction bag. This device has a perineal horseshoe and an optionally perineal forchette. The perineal horseshoe is a “U-shaped” piece with a wide base. The side opposite to the wide base defines a curved surface. The bag is a sleeve folded on itself, producing two concentric tubes. These tubes formed a pair of traction handles. The perineal horseshoe has at least one guide rail and one of the tubes, whether internal or external, have a guide that works in coordination with the herein mentioned guide rail. The perineal forchette consists of a supportive central axis, a handle, a tab and two articulated arms linked to the central axis. The sleeve can have a pair of additional traction handles in its distal end.

Abstract: Coupling device for connecting an annular fixation member to a bone pin, wherein the coupling device comprises pin connecting means arranged for connecting the bone pin to the coupling device and ring connecting means arranged for removably connecting the annular fixation member to the coupling device, wherein the coupling device further comprises fixator connecting means arranged for removably connecting a fixator to the coupling device, wherein the ring connecting means and the fixator connecting means are arranged for simultaneously connecting the annular fixation member and the fixator while the pin connecting means are connected to the bone pin.

Abstract: External fixation systems, and methods for immobilizing joints or fractured bones. An external fixation system may include one or more clamp assemblies connected to one or more rod assemblies at polyaxial joints. Each rod assembly may be length adjustable, and may include a one-way locking mechanism to provisionally lock the length of the rod assembly, and additional locking mechanisms to permanently lock the length of the rod assembly. The system may be deployed pre-assembled as a unit to immobilize a joint or fracture. Another external fixation system further includes a spanning member extending transverse to the rod assemblies. Two or more external fixation systems may be deployed in a stacked configuration on one set of bone pins to immobilize two joints and/or fractures. The systems may be provided in kits including guiding instrumentation, bone pins and pin clamping assemblies for connecting the bone pins to the external fixation systems.

Abstract: A clamping device for attaching to an external fixation element of an external fixation system includes a first jaw having an inner surface and an outer surface and includes a second jaw having an inner surface and an outer surface, with the inner surface of the first jaw and the inner surface of the second jaw together forming a passage configured to receive the external fixation element of the external fixation system. A locking system is engageable with the first and the second jaws. A portion of the locking system is moveable relative to the first and the second jaws between a first position where the locking arrangement is configured to prevent release of the external fixation element having a first size from between the first jaw and the second jaw and a second position where the locking arrangement is configured to prevent release of the external fixation element having a second size from between the first jaw and the second jaw.

Abstract: Growing rod systems and methods for correcting spinal deformities include at least one growing rod assembly and at least one fluid delivery assembly. Each growing rod assembly includes a fluid actuator that is operable to extend first and second rod segments in opposite directions along the spine. The fluid actuator can be provided by, for example, a piston-cylinder actuator. Each fluid delivery assembly includes a fluid pump operably connectable to a fluid line, which in turn is connected to the fluid actuator. In one embodiment, the fluid actuator is of a linear design. In another embodiment, two linear or curvilinear fluid actuators are provided back-to-back and connected by a connecting rod that mounts to the mid-spine and is contourable. In another embodiment, the fluid actuator is of a curvilinear design to generally conform the normal spine. And in another embodiment, the fluid actuator includes a fluid-over-fluid shock absorber.

Abstract: A polyaxial bone screw assembly includes a threaded shank body having an integral shank head receivable in a one-piece receiver having an upper channel for receiving a longitudinal connecting member and a lower cavity cooperating with a lower opening. A compression insert (some with an independent tool lock, lock and release feature and/or friction fit feature) and a split retaining ring articulatable with respect to both the shank head and the receiver (prior to locking) cooperate with the receiver to provide for pop- or snap-on assembly of the shank with the receiver either prior to or after implantation of the shank into a vertebra.

Abstract: The present invention is directed an anchor assembly for use in spinal fixation to interconnect a longitudinal spinal rod with a patient's vertebra. The anchor assembly preferably includes a bone anchor, a body with a rod-receiving channel, an insert member (preferably a bushing), and a locking cap with a saddle. The anchor assembly preferably enables in-situ assembly where the bone anchor may be secured to the patient's vertebra prior to being received within the body of the bone anchor assembly. Accordingly, the anchor assembly enables a surgeon to implant the bone anchor without the body to maximize visibility and access around the anchoring site. Once the bone anchor has been secured to the patient's vertebra, the body may be snapped onto the bone anchor and a spinal rod may be inserted into the rod-receiving channel.

Abstract: A polyaxial bone screw assembly includes a receiver, a shank, an articulation structure for retaining the shank in the receiver and a compression insert for engagement with a longitudinal connecting member such as a rod. The articulation structure includes substantially spherical convex and concave surfaces that slidably engage both shank and receiver surfaces to provide compound articulation between the receiver and the shank. The receiver includes inwardly directed spring tabs engaging the insert and prohibiting rotation of the insert within the receiver.

Abstract: A spinal construct includes a body having a wall disposed between a first cavity and a second cavity. The second cavity being configured for disposal of an existing spinal implant. A rod is disposed with the first cavity and connectable with tissue. The rod is rotatable relative to the body. Systems, surgical instruments, implants and methods are disclosed.

Abstract: A cable bone screw implant and insertion instrument assembly comprising an implantable bone screw having an enlarged head portion. An enlarged head comprises a lock aperture and an insert aperture and holds a deformable stress tube for housing a surgical cable. A lock screw resides in the lock aperture. A control mate on the enlarged head engages with an inserter instrument which comprises an arm rod portion having a driver cannula for housing a locking rod instrument. An end of the elongate rod body is enlarged having a first and second deflector arm. An interlock engages a cable bone screw implant portion. A compression taper on the arm rod portion compresses deflector arms securing the implant. An outer tube housing engages the deflector arms. Sliding the outer tube housing locks or releases the implantable bone screw. A surgical cable is tensioned between two cable bone screw implants for fixation.

Abstract: A bone implant comprising an elongate body having a first end and a second end coupled by a shaft is disclosed. The first portion is configured to couple to a first bone. The second portion comprises a first expandable section comprising at least one expandable feature. The first expandable section is configured to be received within a reverse countersink in a second bone in a collapsed state and to expand within the reverse countersink. The expandable feature couples to a bearing surface of the reverse countersink. A surgical tool comprising a shaft and at least one expandable cutting edge is disclosed. The shaft is sized and configured to be received within a canal formed in a bone. The expandable cutting edge is formed integrally with the shaft. The expandable cutting edge is configured to expand from a collapsed position to an expanded position for forming a reverse countersink.

Abstract: A device, method, and system for treatment or fixation of a fractured, damaged, or deteriorating bone or bones in a mid-foot region. The device comprising an implant with both proximal and distal fastener holes, along with fastener slots in a central elongated body, for securing the implant to the appropriate osseous cortical structures of the foot. The method for treatment or fixation of fractured, damaged, or deteriorating bones in the medial column of the foot with use of a device such as an intramedullary nail that attaches to either the talus or first metatarsal bones to secure the medial cuneiform and navicular bones in place.

Abstract: Systems and methods for bone fixation using a plate straddled by a retainer. In an exemplary system, the plate may be an elongated plate configured to be disposed longitudinally on a bone. The retainer may have a body interconnecting a pair of mounting regions. The body may define a recess, and each mounting region may define a first aperture and a second aperture. The retainer may be configured to be mated with the plate to position a section of the plate in the recess such that the retainer straddles the plate. The first apertures may be configured to define through-axes that are tangential to the bone, to enable use with a line including wire and/or cable, and each second aperture may be configured to define a through-axis that extends through opposite sides of the bone while avoiding a medullary canal thereof, to enable use with a threaded fastener.

Abstract: Various exemplary methods, systems, and devices for blood flow are provided. In general, an implant can be configured to be implanted in bone and to delay clotting of blood flowing from the bone. The implant can include an anti-coagulation agent to delay the clotting of the blood. The anti-coagulation agent can be a coating on the implant, can be natural to a material forming the implant, or can be impregnated into a material forming the implant. In an exemplary embodiment, the implant is implanted in a bone in a surgical procedure for securing a soft tissue to bone, such as a rotator cuff repair procedure or an anterior cruciate ligament (ACL) repair procedure.

Abstract: A surgical system is provided that includes a body extending along a longitudinal axis. A first member is rotatably positioned within the body and includes a first threaded surface. A second member is positioned within the body and includes a second threaded surface that engages the first threaded surface. The second member is non-rotatable relative to the body. A third member is positioned within the first member. An inflatable bone tamp includes an outer shaft coupled to the body, a balloon coupled to the outer shaft and an inner shaft coupled to the third member and the balloon. The first member is rotatable relative to the body to translate the third member along the longitudinal axis to move the balloon from a first length to a second length. Kits and methods are disclosed.

Abstract: A system and method for bending a surgical rod using an automated bending system includes receiving an indication of a plurality of line segments defined on the rod and an indication of an angle measurement to be formed between at least two adjacent ones of the plurality of line segments. Bending parameters to perform on the rod to form the angle measurement between the at least two adjacent ones of the plurality of line segments are determined and operation of the automated bending system is controlled using the bending parameters to create an angle having the angle measurement between the at least two adjacent ones of the plurality of line segments.

Abstract: A system for repairing separated body tissues includes a tensioning device comprising two proximal handles for grasping, a pair of movable distal tensioning tips, a pivot between the proximal handle and distal tensioning tips, and suture holding clamps proximal to the tensioning tips. The tensioning device is used in conjunction with a buckle with lock bars and a tensioning tab for securing and tensioning suture. The tensioning tab is provided to secure the lock bar in its first position until tension on the suture exceeds a predetermined level.

Abstract: An instrument for therapeutically cytotoxically ablating parathyroidal tissue is disclosed. A substance delivery device with which a quantity of an activator substance that is less than a cytotoxic ablation quantity threshold of a parathyroid gland can be percutaneously introduced into parathyroidal tissue is provided. The activator substance, when introduced, is not activated. An energy source device that includes a selector with which a quantity of an energy that is less than a cytotoxic ablation energy threshold of the parathyroid gland can be selected and an energy production device operable to apply the energy to the activator substance is provided.

Abstract: A control circuit for use with an electrosurgical system is disclosed. The control circuit is programmed to provide an electrosurgical signal comprising a plurality of pulses to first and second electrodes and receive a first reading of an impedance between the first and second electrodes. The control circuit is programmed to receive a second reading of the impedance between the first and second electrodes. The control circuit is programmed to determine a difference between the first and second readings and determine that a short circuit is present between the first and second electrodes based on a magnitude of the difference between the first reading and the second reading. The control circuit is programmed to generate a signal indicating the short circuit between the first and second electrodes.

Abstract: A medical member improved in yield is provided. The medical member is assembled with an assembly unit, is movable relative to at least part of the assembly unit, and is provided with: a conductor including a plurality of curved portions and a through hole extending along a plane including the plurality of curved portions; and a coating portion integrally formed with the conductor in such a manner as to cover the periphery of the conductor and fill the interior of the through hole.

Abstract: A medical method is provided, including a medical device having a distal assembly including at least one electrode and at least one treatment element, the medical device generating information regarding at least one of a physiological measurement and an operational parameter of the medical device; a plurality of surface electrodes affixable to a skin of the patient, wherein the surface electrodes are in electrical communication with the distal assembly to obtain position information of the medical device; and a processor pairing the position information and the at least one of a physiological measurement and an operational parameter of the medical device.

Abstract: A laser delivery device may include a connector portion at a proximal end of the laser delivery device and an optical fiber connecting the connector portion to a distal end of the laser delivery device. The connector portion may include a capillary at least partially surrounding a proximal portion of the optical fiber, and the capillary may include dimples on at least a portion of a circumferential surface thereof.

Abstract: The present technology relates to a surgical system, an image processing device, and an image processing method capable of obtaining the posture of an eye more firmly and with a high degree of accuracy. An image information acquisition unit acquires a tomographic image that is a cross-sectional image taken in a direction substantially parallel to an eye axis direction of an eye of a patient. An image recognition unit recognizes each part of the eye on the tomographic image by means of image recognition on the basis of the tomographic image. The control unit calculates the posture of the eye on the basis of the result of recognition of each part of the eye. In this way, by recognizing each part of the eye on the basis of the tomographic image and calculating the posture of the eye on the basis of the result of recognition, the posture of the eye can be obtained more firmly and with a high degree of accuracy. The present technology can be applied to a surgical system.

Abstract: Systems and methods for rendering medical procedures in a virtual reality operating room for a training a trainee are provided. A medical procedure can be simulated and a trainee can manually manipulate a medical tool to perform the simulated medical procedure in virtual reality on a virtual reality avatar in the virtual reality simulation.

Abstract: A system and method for converting static/still medical images of a particular patient into dynamic and interactive images interacting with medical tools including medical devices by coupling a model of tissue dynamics and tool characteristics to the patient specific imagery for simulating a medical procedure in an accurate and dynamic manner by coupling a model of tissue dynamics to patient specific imagery for simulating cerebral aneurysm clipping surgery.

Abstract: A method for implementing a dynamic three-dimensional lung map view for navigating a probe inside a patient's lungs includes loading a navigation plan into a navigation system, the navigation plan including a planned pathway shown in a 3D model generated from a plurality of CT images, inserting the probe into a patient's airways, registering a sensed location of the probe with the planned pathway, selecting a target in the navigation plan, presenting a view of the 3D model showing the planned pathway and indicating the sensed location of the probe, navigating the probe through the airways of the patient's lungs toward the target, iteratively adjusting the presented view of the 3D model showing the planned pathway based on the sensed location of the probe, and updating the presented view by removing at least a part of an object forming part of the 3D model.

Abstract: A method includes receiving multiple measurements, acquired using a registration tool including an ultrasound (US) transducer and a position sensor of a position-tracking system. The measurements are acquired by attaching the tool to multiple locations on a patient head and acquiring position measurements of the position sensor and respective US measurements of bone tissue at the locations. First positions of the bone tissue are calculated based on the position measurement and the US measurements obtained using the registration tool. Second positions of the bone tissue are identified in an anatomical image of the patient head. The anatomical image is registered with a coordinate system of the position tracking system, by correlating the first positions and the second positions, to enable tracking a medical instrument, which is inserted into the patient head and includes another position sensor of the position-tracking system, using the anatomical image registered with the position-tracking system.

Abstract: The present invention can cope with both localized treatment and large-scale invasive surgery and reduces operating time. Provided is a medical system comprising: a first robot arm provided with a first manipulator including a first treatment section and with a first imaging unit having a field of view that includes a movable range of the first treatment section; a second imaging unit having a field of view that is wider than said field of view; a display unit that displays video from the first or second imaging unit; a switching unit that switches the video; an operation unit for inputting operation command for the first manipulator and the first robot arm; and a control unit that controls the first manipulator and the first robot arm on the basis of the operation command.

Abstract: A health monitoring kit includes a package unit, a scale, a display band, and a heart monitor. The package unit includes a base panel with a base face, a first upper panel, and a second upper panel. The first upper panel is connected to the base panel with a first hinge member, and the second upper panel is connected to the base panel with a second hinge member. The scale is retained in the base panel and covers a portion of the base face. The display band is retained in the first upper panel. The heart monitor is retained in the second upper panel.

Abstract: There is provided a medical support device for holding and positioning a needle. This device is particularly useful for positioning needles in a less invasive puncture treatment. This device comprises two rotational elements and at least one needle guide attached to a rotational element and. The needle guide guides the direction of insertion of a needle-like instrument and includes a guide portion that guides a needle or other needle-like instrument where the puncture point of the needle in a first position is different from the puncture point when the needle guide guides the needle in a second position.

Abstract: Medical devices and methods that provide for improved accuracy when positioning of a synthetic structure, such as a MEMS device or a stent, within a biological feature of a patient, such as a blood vessel, are disclosed. A blood vessel sizing device is configured for placement on the skin of a patient near a feature of interest (e.g. a blood vessel to be imaged). The device may include one or more radiopaque elements, including a target element, and one or more positioning markers having known sizes. A clinician may use the radiopaque elements to identify a portion of a blood vessel suitable for positioning of the synthetic structure.

Abstract: Systems, and methods of disassembling systems that includes a medical device, a shaft that is optionally steerable, and a handle assembly. The methods can include providing a system after it has been exposed to a blood environment of a subject, disconnecting a medical device electrical contact from an electrical contact on the printed circuit board, moving the medical distally relative to the sheath and out of the distal end of the sheath, and cleaning at least a portion of the medical device.

Abstract: A method and a medical instrument are disclosed. The medical instrument has a first part comprising an attachment section and a second part comprising one or more functional sections. The medical instrument comprises an identification tag being positioned within the attachment section, and a cover material forming a tube body having at least two openings including a first opening and a second opening. The cover material encloses the identification tag and the attachment section. The first part extends through the first opening and the second opening. The first opening and the second opening are occluded by the first part.

Abstract: Apparatuses and methods for extruding a dental filling material into a tooth. The extrusion is accomplished by harnessing a combination of motor power (such as from an electrical motor) and spring loaded power. This combination overcomes the shortcomings of each of these power sources. In addition, because this combination significantly reduces battery power requirements, it allows for more thermal heating, down-packing, and obturation to be performed than would otherwise be possible.

Abstract: A wedge system for use in a dental restoration procedure for a posterior tooth. The wedge system includes a first wedge including a body, a first arm extending from the body, a second arm extending from the body, and a gap formed between the first arm and the second arm. In some cases, the wedge system may include a second wedge including a body and an arm extending from the body, and at least a portion of the arm of the second wedge can be disposed in the gap of the first wedge to removably secure the second wedge to the first wedge.

Abstract: A wedge for use in a dental restoration procedure for an anterior tooth. The wedge includes a handle portion, a body portion coupled to and extending outward from the handle portion, and a matrix band coupled to the body portion. The body portion is adapted to be disposed in an approximal space between the anterior tooth and a tooth adjacent the anterior tooth. The matrix band is adapted to contact the anterior tooth when the body portion is disposed in the approximal space.

Abstract: Method and system for managing multiple impressions of a patient's jaw for an orthodontic treatment is provided. The method includes scanning at least a first impression and a second impression of same jaw for the orthodontic treatment; determining if the first jaw impression and the second jaw impression have distortion in different areas; selecting the first jaw impression or the second jaw impression as a base impression; and replacing a distorted tooth data from the base impression with data for the same tooth from a non-base impression. The method also includes scanning at least a first jaw impression for the orthodontic treatment; scanning a bite impression for the orthodontic treatment; matching the scanned first jaw impression with the scanned bite impression; comparing bite information with a tooth occlusal surface; and determining if reconstruction is to be performed on the tooth occlusal surface.

Abstract: A system for fabricating a dental restoration to restore a plurality of teeth in a dentition of a patient is described. The dentition includes a restoration dental arch and an opposing dental arch. The restoration dental arch includes a restoration site and the opposing dental arch is opposite the restoration dental arch. The system includes an impression apparatus, a motion capture apparatus, an interference model generation system, and a restoration design system. The impression apparatus is configured to capture an impression of the dentition of the patient. The motion capture apparatus is configured to capture a plurality of location data points that represent the locations of the opposing dental arch relative to the restoration dental arch. The interference model generation system is configured to generate an interference model for the restoration site. The restoration design system is for designing a restoration using the interference model.

Abstract: An additively manufactured dental crown with a wall having a bottom edge and an occlusal portion joined with the wall opposite the bottom edge. The wall and occlusal portion form an interior surface and an opposing exterior surface. By using additive manufacturing and materials for such, the dental crown can have thin walls with a thickness of less than 300 microns at the thinnest portion of it and can include fine printed features such as identifiers, internal ribs, slots, porous meshes, and retention elements.