Abstract: The invention relates to a method for producing a dental prosthesis from a prosthesis base and a plurality of prosthesis teeth, characterized by the following chronological steps: providing the prosthesis teeth and the prosthesis base, wherein the prosthesis base comprises a plurality of tooth sockets for locating the basal surfaces of the prosthesis teeth; applying a plastically deformable connecting means onto the tooth sockets and/or basally onto the prosthesis teeth; locating the prosthesis teeth into the tooth sockets of the prosthesis base and in this situation connecting with the aid of connecting means to the prosthesis base in such a way that the prosthesis teeth, after locating in the tooth sockets, are movable in relation to the prosthesis base, wherein the position and the alignment of the prosthesis teeth to the prosthesis base remain retained if no external force effect is exerted onto the prosthesis teeth; changing the position and/or the alignment of at least one prosthesis tooth in the pro

Abstract: The oral irrigation/liquid delivery device provides flow controlled fluid to body areas specifically the mouth, or parts of body or other non-body areas via pump device or connection to water source through a wand handle with bulbous smooth head with multiple openings/orifices for the fluid to flow to ensure that no high-pressure jets result (unless within the design) and can be used in confined area; idea for irrigating or rinsing the mouth after jaw surgery or other situation where it is not possible or recommended to use a high-pressure “water pick” type of device; allows user who may have a problem sucking in water to rinse to have fluids safely delivered to mouth to clear and clean it; allows for the delivery of medicated and or other liquid delivery of water or any other liquid to rinse or even imbibe; said device could also deliver feeding fluids; optional connection via any pump or faucet diverter system to delivery fluids, including option to have a siphon mix of one solution along with another with

Abstract: An automatic filling mechanism for use in conjunction with a hand-held fluid droplet appliance (10) for dental cleaning, the automatic filling mechanism having a door (42) to a chamber (40) in the hand held fluid droplet appliance (10) for holding fluid, the door having a female liquid inlet port (44) and a female liquid and air exit interface (46) having a snorkel system (80) attached thereto that is inserted into the chamber (40) that is used to fill the chamber (40) with fluid (112) from a reservoir (110) on a docking and charging station (100) when the hand held fluid droplet appliance (10) is inserted into a cradle (160) on the docking and charging station (100).

Abstract: A teeth cleaning travel kit includes toothbrushing mouthpiece that has two inverted channels dimensioned to receive upper and lower bites of dental arches of a user, the channels being integral with one another. Teeth-cleaning bristles inwardly project within the two inverted channels to bear inwardly against teeth and gums of the user, wherein the channels and teeth-cleaning bristles are configured such that mastication produces relative brushing movement of the teeth-cleaning bristles over the teeth and gums. An oral hygiene promoting product is attached to one of the two inverted channels and the teeth-cleaning bristles that is released by action of the user's mouth. The teeth cleaning travel kit also includes a vessel that contains a rinsing fluid and kit packaging that contains the toothbrushing mouthpiece and vessel.

Abstract: An actuator (12) for a personal care appliance (10) having an eccentric core (21) to preload the actuator (12) to prevent rattling caused by detrimental reactionary forces. The eccentric core (21) includes a pole assembly (24) radially extending from a spindle (22) having at least a first set (25-1) and a second set (25-2) of pole members. The first set (25-1) has a greater length as measured from the center of the spindle (22) than the second set (24-2), reducing the magnet gap on one side of the spindle (22) to create an eccentric core and preload the actuator (12). Alternatively, the preload can be mechanically created by a set of bearings (28) disposed within housing (18) of the actuator (12), where the bearings (28) have a centerline (A3) offset from the principal axis (A1) of the housing (18).

Abstract: According to some embodiments of the invention there is provided a dental measuring assembly comprising: an elongated stem defining a longitudinal axis between a proximal end and a distal end of the stem; a measuring abutment configured to be received over the proximal end of said stem and to axially slide over the stem; wherein a distal segment of the stem comprises scale markings denoting a height of a distal end of the measuring abutment relative to the stem. In some embodiments, a plurality of measuring abutments are provided, each abutment defining a different angle relative to the longitudinal axis of the stem.

Abstract: A vertical dimension of occlusion jig includes a vertical support column, a lateral arm support base configured to slide along and rotate about a longitudinal axis of the vertical support column, a first lateral support arm pivotally coupled with the lateral arm support base, a first tooth gantry coupled with the first lateral support arm and adapted to slide along and rotate about a longitudinal axis of the first lateral support arm, a second lateral support arm pivotally coupled with the lateral arm support base, and a second tooth gantry coupled with the second lateral support arm and adapted to slide along and rotate about a longitudinal axis of the second lateral support arm. A temporary anchorage device (TAD) gantry is coupled with the vertical support column and is configured to slide along a longitudinal axis that is perpendicular to the longitudinal axis of the vertical support column.

Abstract: The present invention relates to an inhalation toxicity testing chamber device for nanoparticles having a plurality of concentrations. The present invention provides an inhalation toxicity testing chamber device for nanoparticles having a plurality of concentrations, which: can supply nanoparticles having different concentrations to particle exposure modules by stacking a plurality of particle exposure modules inside a single chamber housing and by allowing each particle exposure module so as to form an independent space from each other; can perform inhalation toxicity testing of nanoparticles having a plurality of concentrations through a single chamber housing by being capable of exposing the test animals put into each particle exposure module to nanoparticles having different concentrations; can easily perform inhalation toxicity tests of nanoparticles in a small scale laboratory etc.

Abstract: One aspect of the present disclosure relates to a tissue repair implant comprising a first layer of extracellular matrix and a second support layer of biocompatible material securely attached to the first layer at one or more fixation points. At least one of the fixation points comprises a first projection that is associated with the first layer and securely attached, via a fixation mechanism, to the second support layer.

Abstract: Soft tissue grafts, packaged soft tissue grafts, and methods of making and using soft tissue grafts are disclosed. One soft tissue graft includes processed tissue material having first and second opposed surfaces. The first and second opposed surfaces are bounded by first and second edges. The first edge has a concave shape that curves toward the second edge. The second edge has a convex shape that curves away from the first edge. The first surface comprises a plurality of apertures. At least one of the apertures is formed from a multi-directional separation in the first surface. One method of making a soft tissue graft includes positioning a cutting die on a surface of tissue material, pressing the cutting die into the tissue material to cut the tissue material, and processing the cut tissue material to create processed tissue material.

Abstract: Embodiments of the present disclosure provide a removable embolic protection device for deployment at a body vessel, as well as systems and methods for implanting the device within a vessel of a patient.

Abstract: Human implantable tissue expanders are provided, such as breast tissue expanders, that comprise an inner foam filling enclosed within a liquid-filled compartment and further within a sealing shell comprising a substantially non-stretchable resilient expansion restricting layer. The substantially non-stretchable resilient expansion restricting layer is configured to retain a shape and/or volume of said foam filling upon changes of ambient pressure and/or temperature.

Abstract: Methods, devices, and systems for mechanically reducing the volume of the lung. Some embodiments include endobronchially positioning an anchoring device within a lung, the anchoring device comprising at least a distal anchor, expanding at least a portion of the distal anchor to anchor the distal anchor against lung lumen tissue, and tensioning at least a portion of the device to reduce the volume of the lung.

Abstract: An aortic arch device that is a unitary tube of graft material having a crimped unstented portion and a stented portion, a collar at the junction of the crimped unstented portion and the stented portion, at least one fenestration or lateral opening in the graft material to accommodate arteries in the aortic arch. Branches may extend from the fenestrations.

Abstract: Described herein is a simplified placement system and method for a tissue graft anchor by which a surgeon may introduce one or more sutures into a hole in a boney tissue, apply a precise amount of tension to the sutures to advance a soft tissue graft to a desired location, and then advance the anchor into the bone, preferably while maintaining the requisite pre-determined suture tension and without introducing spin to the suture. Particularly preferred embodiments allow for the one-handed operation. To that end, embodiments in which relative axial movement between the inner tensioning device and outer driver device is optionally physically constrained, for example by means of cooperating and/or compressive elements disposed in the respective hub and handle portions, are described herein.

Abstract: A device for prosthetic vision rehabilitation, which includes a scleral explant with a shape that is suitable for being in contact with at least one portion of the sclera of an eye, and at least one inducer arranged on the scleral explant.

Abstract: A method of inserting and securing a corneal implant in engaging and fluid-flow limiting relation to the posterior cornea, such as to treat edema. The method includes securing a corneal implant in fluid flow limiting relation to the posterior cornea through an incision in the eye and securing it in place by a variety of steps such as corneal insertion or laser bonding, and preferably by inserting a removable corneal implant including a central region and a plurality of retention member(s) disposed on the periphery thereof into the eye so as to releaseably and removably engage a portion of the eye and thereby retain the corneal implant in abutting and engaging relation with the posterior cornea. The retention members of the corneal implant may also comprise haptic leg(s) extending from the central region.

Abstract: Techniques and mechanisms for the wireless transmission of power and sensor information between two components of an implantable ophthalmic device are disclosed herein. An example device includes an accommodating intraocular lens (aIOL) and separate auxiliary electronics, both enclosed in biocompatible materials. The aIOL includes a dynamic optic, control logic, a battery and an antenna. The auxiliary electronics include an antenna, an energy storage cell, and a sensor. The auxiliary electronics may be wirelessly coupled to the aIOL for the wireless transmission of power and sensor information.

Abstract: An intraocular lens (IOL) insertion apparatus may include a handpiece body having a distal tip and a deployment chamber located at a distal end of the handpiece body. The deployment chamber is sized and shaped to hold a folded IOL. The IOL insertion apparatus further includes a deployment system disposed within the handpiece body. The deployment system may include a deployment carriage movable between a first position and a second position within the handpiece body. The deployment carriage may include a biasing element that biases the deployment carriage in a distal direction toward the distal tip. The deployment system may further include a deployment trigger that prevents distal movement of the deployment carriage unless pressed and a deployment plunger having a proximal end secured to the deployment carriage and a distal end to engage the folded IOL.

Abstract: An intraocular lens (IOL) insertion apparatus may include a hand piece body having a distal tip, an IOL folding chamber, and IOL a dwell position, and a telescoping plunger having a first plunger portion and a second plunger portion. The first plunger portion and second plunger portion may be arranged to simultaneously advance through a first portion of a displacement of the telescoping plunger, and one of the first and second plunger portions may be arranged to advance through a second portion of the displacement of the telescoping plunger.

Abstract: An intraocular lens (IOL) insertion apparatus includes a handpiece body having a distal tip and a proximal section. The IOL insertion apparatus also includes a folding chamber located within the handpiece body, the folding chamber shaped to fold an IOL advancing through the folding chamber. The IOL insertion apparatus also includes an advancement system. The advancement system includes an advancement carriage movable between a first position and a second position within the handpiece body. The advancement carriage includes a spring system biasing the advancement carriage in a distal direction toward the second position and a dampening system to dampen motion of the advancement carriage. The advancement system further includes an elongated advancement plunger that includes a distal end to advance the IOL through the folding chamber and a proximal end connected to the advancement carriage.

Abstract: This disclosure describes, inter alia, materials, devices, kits and methods that may be used to treat chronic sinusitis.

Abstract: A method for treating a patient may include establishing an anastomosis between a pulmonary artery and an aorta; and pumping blood from the pulmonary artery to the aorta when the pulmonary artery has a pressure lower than or equal to a pressure of the aorta.

Abstract: Embodiments of a crimping device for crimping a radially expandable and compressible prosthetic valve are disclosed. A crimping device can comprise a housing configured to receive a prosthetic valve in a radially expanded state. The housing member can include a funnel segment and an outlet in communication with the funnel segment. The crimping device can further comprise an actuator rotatably coupled to the housing, wherein rotation of the actuator relative to the housing causes the prosthetic valve to move axially through the funnel segment such that at least a portion of the prosthetic valve compresses radially by engagement with the funnel segment and exits the crimping device via the outlet.

Abstract: A device for artificial cardiac valve support, the device including an upstream portion designed to expand to have at least one dimension wider than a native heart valve annulus, a downstream portion attached to the upstream portion, the downstream portion also designed to expand to have at least a portion with at least one dimension wider than a native heart valve annulus, and a plurality of artificial valve commissure posts. A method for producing a device for artificial cardiac valve support, the method including producing an upstream portion, producing a downstream portion, and attaching the upstream portion to the downstream portion, producing a frame for artificial cardiac valve support. Related apparatus and methods are also described.

Abstract: A tubular portion of a valve frame circumscribes a longitudinal axis, and defines a lumen along the axis and a plurality of valve-frame coupling elements disposed circumferentially around the axis. An outer frame: (a) comprises a ring defined by a pattern of alternating peaks and troughs, the pattern having an amplitude, (b) comprises a plurality of legs, coupled to the ring at respective troughs, and (c) is shaped to define a plurality of outer-frame coupling elements, each coupled to the ring, and fixed with respect to a respective valve-frame coupling element. Compression of the tubular portion from an expanded state toward a compressed state reduces a circumferential distance between each of the outer-frame coupling elements and its adjacent outer-frame coupling elements, and increases the amplitude of the pattern of the ring.

Abstract: The disclosure provides insertion tools and articles that facilitate entry of a medical device, such as a balloon catheter, into the body. In embodiments the insertion tools have an elongate hollow body (50) that is able to protect a portion of a medical device, such as a balloon of a balloon catheter, during an insertion procedure. In one embodiment the insertion tool has an elongate hollow body (131), a tapered distal end (135), and a locking mechanism (133) at the proximal end which can secure a portion of a balloon catheter. An opening at the distal end can allow passage of the balloon in a folded uninflated state.

Abstract: Apparatus is provided for adjusting at least one dimension of an implant. The apparatus includes a rotatable structure having a channel extending between first and second openings of the rotatable structure. The channel is configured for passage therethrough of an elongate tool. The rotatable structure has a lower surface that is shaped to define a first coupling. The apparatus includes a mechanical element having a surface coupled to the lower surface of the rotatable structure. The mechanical element is shaped to provide a second coupling configured to engage the first coupling during a resting state of the mechanical element, in a manner that restricts rotation of the rotatable structure. The mechanical element has a depressible portion that is disposed in communication with the second opening, and is configured to disengage the first and second couplings in response to a force applied thereto by the elongate tool.

Abstract: Embodiments of the present technology include a graft for administration at a treatment site of a patient. The graft may include a human cadaveric bone material bonded together with a polymeric binder. The human cadaveric bone material may include demineralized bone particles. The demineralized bone particles may have an average diameter less than 1.1 mm, less than 750 ?m, less than 500 ?m, or less than 250 ?m. The human cadaveric bone material may include non-demineralized bone, cancellous bone, and/or cortical bone in embodiments. In some embodiments, bone from animals other than humans may be used, and the patient may be an animal other than a human.

Abstract: An orthopedic medical implant, implant part or surgical instrument includes a metallic body having a metal or a metal alloy. The metallic body includes a sub-surface that is a thermal diffused boron carbide layer, and the metallic body is void of an additive layer onto a surface of the metallic body.

Abstract: A method of preparing an interpositional implant suitable for a knee. The method includes determining a three-dimensional shape of a tibial surface of the knee. An implant is produced having a superior surface and an inferior surface, with the superior surface adapted to be positioned against a femoral condyle of the knee, and the inferior surface adapted to be positioned upon the tibial surface of the knee. The inferior surface conforms to the three-dimensional shape of the tibial surface. The implant may be inserted into the knee without making surgical cuts on the tibial surface. The tibial surface may include cartilage, or cartilage and bone.

Abstract: A method and apparatus are provided for making a temporary hip joint prosthesis. The method includes horizontally positioning each half of a two-part mold having a respective impression of a front side and a backside of a hip joint prosthesis. The method includes level filling the selected impressions with a bone cement mixture. The method includes rotating one half of the two-part mold to align the front side and back side of the hip joint prosthesis. The method includes maintaining the two halves of the two-part mold in contact as portions of the bone cement mixture in each half adhere together and cures. The method includes removing a hip joint prosthesis from the two-part mold.

Abstract: A veterinary hip resurfacing prosthetic system includes a femoral cap and an acetabular cup. The cup shell has a thickness of less than 2 mm and a liner in the shell has a thickness of less than 2.5 mm in order to accommodate a larger femoral cap. Further included are features for preventing rotation of the liner relative to the shell, for releasably locking the liner in the shell, and for accessing the liner to remove it from the shell.

Abstract: An elbow prosthesis includes a stem structure and an articulating component. The stem structure is operable to be positioned in a bone of a joint and includes a stem portion and a C-shaped body portion. The stem portion is operable to be positioned in the bone. The C-shaped body portion includes a first articulating surface bound by a medial wall and a lateral wall. The medial and lateral walls are separated by a first distance. The articulating component includes a second articulating surface positioned between a medial side surface and a lateral side surface. The medial and lateral side surfaces are separated by a second distance that is less than the first distance. The second articulating surface is configured to slidably communicate in a medial/lateral direction along the first articulating surface of the C-shaped body portion.

Abstract: An elbow prosthesis according to the present teachings can include a stem structure and an articulating component. The stem structure can be operable to be positioned in a bone of a joint. The stem structure can include a stem portion that is operable to be positioned in the bone and a C-shaped body portion having a first retaining mechanism formed thereon. The articulating component can have a second retaining mechanism formed thereon. One of the first and second retaining mechanisms can comprise an extension portion and a first anti-rotation portion. The other retaining mechanism can comprise a receiving portion and a second anti-rotation portion. The articulating component can be advanced from an insertion position to an assembled position, such that the first and second mechanisms cooperatively interlock to inhibit translation and rotation of the articulating component relative to the C-shaped body portion of the stem structure.

Abstract: The present invention relates to cruciate ligament retaining knee implants, and instruments and methods for implanting cruciate ligament retaining knee implants.

Abstract: Methods and devices for correcting wear pattern defects in joints. The methods and devices described herein allow for the restoration of correcting abnormal biomechanical loading conditions in a joint brought on by wear pattern defects, and also can, in embodiments, permit correction of proper kinematic movement.

Abstract: Prosthesis for a shoulder joint including a humeral component equipped with a stem, a head component and connection or articulation means of the humeral component with the head component, wherein the prosthesis according to the invention can be used both as a conventional prosthesis and as a reverse-type prosthesis.

Abstract: This set comprising: an anatomic articulating member, having a concave articulating surface intended to articulate with a complementary humeral implant and having an anatomic coupling feature, a reversed articulating member, having a convex articulating surface intended to articulate with a complementary humeral implant and having a reversed coupling feature that is shaped differently from the anatomic coupling feature, and an anchorage member intended to be anchored in a human glenoid, the anchorage member including a body which defines a proximodistal axis and has inner bore extending along the proximodistal axis, the body being provided within the inner bore with both an inner first feature that is designed to cooperate with the anatomic coupling feature when the anatomic coupling feature is introduced within the inner bore, so as to fixedly couple the anchorage member with the anatomic articulating member, and an inner second feature that is designed to cooperate with the reversed coupling feature when

Abstract: An ankle prosthesis has a tibial component configured for attachment to a tibia of a person, and a talar component. The talar component has a first surface configured for facing the tibial component and a second surface configured for facing a talus of the person. The second surface has first and second arms attached to it, for pivoting or flexing outwardly in medial and lateral directions, respectively, to engage side surfaces of a previously formed slot in the talus.

Abstract: The present technology relates generally to devices and methods for arthroplasty procedures. In some embodiments, for example, a device is disclosed for use during an arthroplasty procedure of a joint of a patient, the joint extending between a first joint end of a first bone and an abutting second joint end of a second bone of the patient. The device includes an end plate configured and arranged for disposing over the first joint end of the first bone, a longitudinal plate extending from the end plate and configured and arranged for disposing along a medial, longitudinal surface of the first bone, and a stem extending from the end plate and suitable for extending along an intra-medullary canal of the first bone. When installed, at least one fastener extends at least partially through the first bone and couples the longitudinal plate to the first bone.

Abstract: A spinal facet fusion implant comprising: an elongated body having a distal end, a proximal end and a longitudinal axis extending between the distal end and the proximal end, the elongated body being characterized by a superior body surface and an inferior body surface; a superior stabilizer extending outwardly from the superior body surface, the superior stabilizer being characterized by a superior stabilizer surface; and an inferior stabilizer extending outwardly from the inferior body surface, the inferior stabilizer being characterized by an inferior stabilizer surface; wherein (i) the superior body surface and the inferior body surface are tapered relative to one another, and/or (ii) the superior stabilizer surface and the inferior stabilizer surface are tapered relative to one another.

Abstract: Intervertebral implants, assemblies, and methods thereof. An intervertebral implant includes opposing chamfered edges to reduce a diagonal distance between the edges. The reduced diagonal distance minimizes distraction of an intervertebral disc space during insertion of the implant. A tool for insertion and rotation of the implant is also provided.

Abstract: A spinal implant comprising an upper and a lower end plate connected by inner and outer lateral walls, said outer lateral walls forming an anterior wall, a posterior wall and two longitudinal walls, said inner lateral walls encompassing a receiving space, and engagement elements being arranged on and projecting from said upper and lower end plates. According to the invention, in order to avoid wear and abrasion when implanted and to improve ingrowth of the spinal implant into the tissue, said spinal implant consists of a ceramic material and carries a porous ceramic foam in at least some sub-sections.

Abstract: An expandable implant includes a base member including a top surface, a first end, and a second end, and defining a central cavity positioned between the first end and the second end; an adjustable member including a top surface and at least one control channel, wherein the adjustable member is adjustably coupled to the base member and movable between a first, collapsed position, and a second, expanded position; a control shaft rotatable received by the base member, wherein rotation of the control shaft cause relative movement of the adjustable member relative to the base member; and at least one control member received on the control shaft and by the control channel, wherein rotation of the control shaft causes the control member to translate along the control shaft and along the control channel.

Abstract: The embodiments provide various interbody fusion spacers, or cages, for insertion between adjacent vertebrae. These intervertebral cages can restore and maintain intervertebral height of the spinal segment to be treated, and stabilize the spine by restoring sagittal balance and alignment. The cages may have a first, insertion configuration characterized by a reduced size at each of their insertion ends to facilitate insertion through a narrow access passage and into the intervertebral space. The cages may be expanded to a second, expanded size once implanted. In their second configuration, the cages are able to maintain the proper disc height and stabilize the spine by restoring sagittal balance and alignment. The intervertebral cages are configured to be able to adjust the angle of lordosis, and can accommodate larger lodortic angles in their second, expanded configuration. Further, these cages may promote fusion to further enhance spine stability by immobilizing the adjacent vertebral bodies.

Abstract: The embodiments provide various interbody fusion spacers, or cages, for insertion between adjacent vertebrae. The cages may contain an articulating joint to allow expansion and angular adjustment, and enable upper and lower plate components to move relative to one another. The cages may have a first, insertion configuration characterized by a reduced size at each of their insertion ends to facilitate insertion through a narrow access passage and into the intervertebral space. In their second, expanded configuration, the cages are able to maintain the proper disc height and stabilize the spine by restoring sagittal balance and alignment. The intervertebral cages are able to adjust the angle of lordosis, and can accommodate larger lodortic angles in their second, expanded configuration. Further, these cages may promote fusion to further enhance spine stability by immobilizing the adjacent vertebral bodies.

Abstract: The embodiments provide various interbody fusion spacers, or cages, for insertion between adjacent vertebrae. The cages may contain an articulating mechanism to allow expansion and angular adjustment, and enable upper and lower plate components to glide smoothly relative to one another. The cages may have a first, insertion configuration characterized by a reduced size at each of their insertion ends to facilitate insertion through a narrow access passage and into the intervertebral space. In their second, expanded configuration, the cages are able to maintain the proper disc height and stabilize the spine by restoring sagittal balance and alignment. The intervertebral cages are able to adjust the angle of lordosis, and can accommodate larger lodortic angles in their second, expanded configuration. Further, these cages may promote fusion to further enhance spine stability by immobilizing the adjacent vertebral bodies.

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

Abstract: This system comprises: at least one vibrational sensor which is operable to produce data each time an impact application device applies an impact from a user to the prosthetic component during assembly between the prosthetic component and with the support member, the produced data representing acoustic vibrations generated in the air and/or material vibrations generated in the impact application device, an analysis unit which is configured both to calculate a frequency characterization of the vibrations for each impact applied by the impact application device to the prosthetic component, from the corresponding data produced by the at least one vibrational sensor, and to compare the frequency characterizations that are respectively calculated for successive impacts so as to provide at each of the successive impacts either a first indication when the assembly between the prosthetic component and the support member is not fully seated or a second indication when the assembly between the prosthetic component and