Patent Application
20210068931
The invention lies in the field of dental implant systems.
So-called single-part and so-called two-part implant systems are known amongst dental implant systems.
In single-part dental implant systems, the actual dental implant—which is implanted into the jawbone and serves for anchoring a functional superstructure, for example, a crown, a bridge or a prosthesis—has a structure that is accessible from coronally after the implantation and on which the attachment part can be fastened in a direct manner.
In two-part dental implants, apart from the actual implant (also called “anchoring part” or “screw” if it is provided with a thread), an abutment, which is envisaged for fastening to this actual implant is necessary. Here, the anchoring part can be designed such that it is introduced in a manner in which it is approximately flush with the bone surface (as a so-called bone-level implant) or, coronally of the bone surface it can be provided with a region that is often widened with respect to the enossal region that is generally provided with a thread, the first-mentioned region sometimes being termed a “tulip” and being envisaged to reach roughly up to the gum surface. Implants with such a transgingival region are called tissue-level implants. In two-part implant systems, the region (“post”) that projects out of the gums and that serves for fastening a superstructure, thus a crown, bridge, prosthesis or the like is formed by the abutment.
The implants that are to be screwed into the bone have gained a high popularity in the case of single-part implant systems as well as two-part implant systems. A relatively controlled implantation is possible by way of such implants, and the outer thread of the implant creates at least some degree of primary stability.
Despite this certain degree of primary stability, the implantation process is very cumbersome and protracted. Firstly, after the extraction of the tooth that no longer fulfils its function, one must wait for a relatively long time until the bone has regenerated again at the location of the extraction to such an extent that it is sufficiently stable for an implant that is to be subsequently implanted. A hole is subsequently drilled at the location of implantation, and the implant is introduced. A multi-month healing-in phase, during which the implant is not mechanically loadable is subsequent to this. Concerning sub-gingival (bone level) implants, the gums are closed above the implant during this healing-in phase, whereas a suitable protection must be attached in the case of other implants. Only after the healing-in phase is the final provision with an abutment and crown, bridge or prosthesis effected, possibly after a renewed opening of the gums.
It has also been suggested, for example, in WO 2013/124260, to have a dental implant mass-produced in a shape that is adapted to the extracted tooth and to insert it directly into the extraction alveolus (extraction socket) after the extraction of the tooth. With this approach, there is no waiting time for the post-growing of the bone. However, on account of the non-round cross section, the dental implant can only be implanted by way of knocking in, which is why only a very small primary stability is possible after the implantation. For this reason, in WO 2103/124260 it is suggested, after implantation, to fasten the implant on an adjacent tooth by way of a device that is specially envisaged for this. Despite this, after the healing-in, a further treatment step is necessary, by way of the fastening having to be removed and the final crown only then being able to be placed. Neither does the procedure according to WO 2013/124260 solve the problem of a longer bone regeneration phase being necessary between the treatment steps.
Amongst other things, a dental implant that consists of a thermoplastic or thixotropic material is known from WO 02/069 817. For anchoring, this material is pressed apically into the jawbone in a linear movement amid ultrasonic vibrations, by which means it is pressed in the flowable condition into the pores of the bone and is anchored there. Towards the coronal side, it has a structure, into which an artificial tooth can be screwed. With such a system, the orientation of the implant after implantation must be defined if the artificial tooth is shaped in an anatomically meaningful manner. WO 2004/017857 also teaches implants, amongst these dental implants, concerning which an anchoring in the bone is accomplished by way of liquefaction of thermoplastic or thixotropic material and the subsequent solidification in a condition, in which the bone tissue is interpenetrated. According to WO 2004/017857, additionally to thermoplastic or thixotropic material, the implant includes a part that forms a surface region of a non-liquefiable material, the region remaining free of liquefied material even after implantation. Similarly, WO 2005/079696 also teaches such implants, which, however, are characterised in that bone tissue is removed apically by way of the linear movement on introduction, by way of the implant including cutting edges in order create a cavity in the first place, into which cavity the implantation is effected. WO 2005/079696 also teaches embodiments, in which thermoplastic or thixotropic material is brought into a cavity and after liquefaction penetrates from this cavity through exit openings into the surrounding tissue. WO 2005/079696 teaches sealingly closing this cavity after implantation. Finally, according to WO 2011/054122, surgical implants are anchored by way of thermoplastic material that in a flowable condition is pressed into the bone, wherein the surgical implant forms a sleeve with a longitudinal opening, into which a thermoplastic element is inserted and against whose distal end the element is pushed for the liquefaction.
The anchoring of the dental implants according to WO 02/069 817, WO 2004/017857 and WO 2005/079696 is advantageous since the dental implants are anchored in a stable manner directly after the implantation and the anchoring is immediately loadable, which in comparison entails significant advantages for the patient. However, the use of these implants also generally entails a longer bone regeneration time at least before the implantation. WO 2005/079696 describes approaches with a view to solving these problems, but such approaches are not suitable to the same extent for all implantation situations and moreover entail the naturally compacted bone tissue around the extraction alveolus being removed.
It is an object of the invention to provide a dental implant and a dental implant system that overcomes the disadvantages of the state of the art, and which, in particular, permit an implantation with an immediate primary stability and/or a high anchoring stability without having to accept the disadvantages of the related state of the art.
According to a first aspect of the invention, a dental implant is provided, the implant including:
According to the first aspect of the invention, the implant is optimised with regard to the anatomical implantation situation and/or is designed for the immediate implantation in the extraction alveolus. For this purpose, it has, for example, a non-round shape, i.e. it is not rotationally symmetrical about the coronal-apical axis. Additionally or as an alternative, it includes one or more of the following features:
The features can be realised on their own or are arbitrarily combinable, wherein given a combination of the features A and D, feature A is only to be understood for the region coronally of the cutting edge (in other embodiments the steplessness applies to the complete enossal region). All other combinations are possible without limitation, wherein synergy effects can result as is yet described hereinafter.
Thus altogether, apart from the realisation of one of the features on its own, all combinations are also possible, therefore AB, ABC, ABCD, ABCDE, ABCE, ABD, ABDE, ABE, AC, ACD, ACE, ACDE, AD, ADE, AE, BC, BCD, BCE, BCDE, BD, BDE, BE, CD, CE, CDE, DE (all permutations).
In particular, the exit openings are relatively far apically and, inasmuch as several are present, are arranged on a same level. The latter means that there are not several levels of exit openings, i.e. that several exit openings are not arranged above one another at a position that corresponds to one another in the peripheral direction.
The approach according to the mentioned aspect of the invention renders it possible for the implant to be inserted into the extraction alveolus directly after implantation and to be anchored there, and specifically permanently on account of the thermoplastic material (if the material is not resorbable) or at least until the osseointegration has advanced sufficiently far, in order to anchor the implant by way of ingrowth (if the material is resorbable). A disadvantage of those implants that are adapted in their shape to the extraction alveolus and are anchored into this by way of knocking in is overcome by way of this. Specifically, it has been found that although an anchoring in the bone via a press fit is capable of being quite stable directly subsequent to implantation, the connection via the press fit however becomes weaker in the following weeks.
The approach of the invention does not rule out the implantologist not placing the implant until after the bone regeneration phase, thus not implanting it directly into the extraction alveolus. Even then, the approach according to the invention is still advantageous and an implant shape that is much better adapted to the anatomy can be selected due to the shape, which does not necessarily have to be rotationally symmetrical and cylindrical or conical, and the long-term stability is therefore significantly encouraged.
The implant body can also be slightly over-dimensioned according to the procedure according to the invention, i.e. the external dimensions are slightly larger than the dimensions of the cavity (extraction alveolus or the opening in the bone, which is created at a later stage), so that on introduction (then, for example, by way of knocking in) into the cavity, the implant body is pressed into this and also held by a press fit.
A cross-sectional shape, which reduces apically in a stepless manner according to feature A, imitates the anatomic shape of the root and therefore permits an optimal adaptation to the anatomical conditions. In particular, the shape can be such that the line of the centre of gravity (axial course of the centre of gravity of the horizontal section surface) is arcuate, however, for example, without the outer surface of the implant forming an undercut in the enossal region.
The implant body of an implant with feature A in particular can have a surface shape that is continuous in the enossal region and which is without ribs or channels, with the exception of an optional surface roughness, which is over the whole surface or is selectively present and which encourages osseointegration. However, the presence of axially, i.e. longitudinally running ribs and/or channels is also not ruled out. An additional retention can therefore be effected by way of the compression of the outer edges that are formed by the ribs given implant materials (for example, metallic implant materials), which tend to be softer. In the case of harder implant materials, the bone tissue will yield at the location of the ribs, and the arising structure will contribute to an additional mechanical anchoring.
Very generally, the outer implant surface all in all can be rough in the enossal region, wherein a roughness can be present over the whole surface or selectively only at some locations. As is known per se, the surface roughness can be produced by a material-removing method (sand blasting, laser ablation) and/or a deposition method (coating). The osseointegration can also be encouraged by the selection of matching chemical characteristics of the surface (coating).
A cross-sectional shape according to feature B can be elliptical, approximately polygonal (for example, with rounded corners), multi-lobed, etc. In the case of an implant with a non-round cross section, such a cross-sectional shape firstly permits the thermoplastic material to predominantly lie closer to the provided exit opening, and specifically already in the initial condition before the liquefaction.
The feature moreover permits an optimal design/fashioning of the wall thicknesses of the implant body even given comparatively large ratios between the volume of the cavity and the outer cross section of the implant body, which is inherently limited by the anatomy.
The cross-sectional shape of the thermoplastic element can be matched in particular to the cross-sectional shape of the cavity, by way of the thermoplastic element in the solid condition essentially completely filling the cavity in an axial region when it is inserted into the cavity or fills this out from the very onset. Supplementarily or alternatively, a distal end of the sonotrode, with which the liquefaction is effected can have an adapted cross section. By way of this, a back-flow of thermoplastic material coronally can also be prevented when, during the method, the thermoplastic element is liquefied up to the coronal end.
Feature C is firstly based on the recognition that an anatomically optimally adapted implant can also be provided for the replacement of teeth with multi-canal roots. It is therefore not necessary, as is envisaged in the state of the art, to implant an implant with a cross section, which in the region of the middle of the dental root, is accordingly slightly enlarged in comparison to a single root canal, this not being adapted to the natural anatomical conditions, but the implant can be designed almost as the naturally grown one, particularly as the natural dental root shape also at the most forms a slight undercut and can therefore be well approximated by a shape, which is implantable by way of a movement in the axial direction (also—and this applies generally to embodiments of the invention—a slightly undercut implant body shape is moreover possible, particularly as the thermoplastic material can fill cavities, which possibly arise by way of this and can therefore compensate dimensions). Secondly, feature C is based on the recognition that the anchoring by way of thermoplastic material is almost ideally compatible with a corresponding multi-canal root shape, by way of cavities or sub-cavities being able to lead into the various canals and thus ideally assisting a depth-effective anchoring. This can also be particularly advantageous since the bone tissue is generally more cancellous at a greater depth and includes more cavities, into which the liquefied thermoplastic material can flow, in order to form an anchoring after re-solidification.
If the implant is inserted directly into the extraction alveolus, then depending on the patient, the situation in which the bone tissue directly around the alveolus is very compact arises. This on the one hand has the advantage of a very large mechanical stability of the bone tissue that supports the implant. On the other hand, there is the possible disadvantage of comparatively little thermoplastic material being able to penetrate into the bone tissue and the related anchoring under certain circumstances would remain superficial. For this purpose, a method for the implantation of an implant of the claimed type described in this text, the method likewise belonging to the invention, envisages the bone tissue being removed only locally where the exit openings later lie. This can be accomplished by the experienced implantologist by hand with a suitable drilling tool or punching tool. Alternatively, adapted aids with a function that guides the user can also be used. For example, a non-rotating machining tool that has an outer shape, which is adapted to the extraction alveolus, and on account of this, can be introduced into this alveolus in an orientation, which is defined with respect to this can be used. Such a tool can be configured to remove bone tissue locally at the location of the exit openings, for example, by way mechanical oscillations being coupled therein.
As a further alternative, the implant can be configured such that on implantation, it itself clears away the compacted bone tissue in a very local manner. According to feature D, this is effected with a cutting edge, which is provided apically of the exit opening—and only there. In particular—but not only—with embodiments with feature D, one can envisage the exit opening or the exit openings lying in a region, in which the implant body has an apically pronouncedly tapering shape. By way of this, the cutting edge, which lies apically of the exit opening, only engages into the bone tissue when the implant body has already penetrated far into the alveolus, and the region that is cleared of the compact bone tissue is limited to the region in the direct proximity of the exit opening.
Such a cutting edge can run in an essentially horizontal manner, i.e. parallel to a plane that is perpendicular to the coronal-apical axis. It can also run obliquely, but not parallel to the coronal-apical axis. However, in contrast to approaches according to the state of the art, the cutting edge will not be peripheral, but restricted to the location of the exit opening, i.e. it is only as wide as the exit opening or insignificantly wider.
Such a cutting edge can also run in an essentially plough-like, i.e. V-shaped manner. In particular, it is suitable for grinding up the compacted bone tissue around the exit opening. Ground-up bone tissue (bone fragments, amongst these also fine grains), which arises due to this, can also be cemented, i.e. shaped into a common solidified mass, by way of the exiting thermoplastic material.
Feature E utilises the fact that implants are already loadable to a certain degree directly after implantation. According to the first option, apart from the implant with the implant body and thermoplastic element, the implant system can also include a separate crown that can be placed onto the step, as well as optionally a gingiva former that can be applied before placing the crown. According to the second option, the crown can be present directly as one part with the implant, i.e. the implant as a whole forms an artificial tooth with a root and crown. Cement, which is envisaged for dental applications, can be used, for example, for closing the cavity or the cavities. The crown can be individually manufactured, according to both options.
According to a first option, the implant body itself can likewise be manufactured individually and this applies generally to implants according to the invention. This can be effected in a manner known per se by way of a computer-based method based of 3D-data (3D-printing). The 3D-data, which is used for the method, is based on measurement data that is taken from the patient, wherein this data is adapted manually or by way of software so that a cavity or a plurality of cavities with the characteristics described in this text is fitted in.
According to a second option, a plurality of implant bodies, which are adapted to the natural tooth root shapes, and corresponding thermoplastic elements are provided, for example, in different sizes. The implantologist then selects an implant in accordance with the implantation position. The invention also includes an implant set with a selection of premanufactured implants for different implantation situations. Such an implant set in particular can include implants with only one root canal as well as implants with several root canals, for example, with two and with three root canals.
The thermoplastic material of the thermoplastic element can be resorbable, for example, by way of it being composed on the basis of polylactide. The thermoplastic material then serves merely for the primary stabilisation, whereas the bone, which has grown into the structures of the lateral surface, then later assumes the stabilisation. The bone can then also grow into the exit openings, which yet further increases the mechanical stability. Alternatively, the thermoplastic element can also consist of a non-resorbable material, for example, PMMA or a polyamide. There is a large selection of resorbable materials as well as non-resorbable materials that are suitable for the implantation, and the invention is not restricted to certain materials.
The implant body can be ceramic. The procedure according to the invention is particularly favourable for implant bodies of ceramic materials since it permits the available space to be utilised in an almost optimal manner and the wall thicknesses of the implant to be homogeneous, so that the breakage strength can be optimised.
However, the procedure according to the invention can be used just as well for implant bodies of metallic materials, for example, materials based on titanium.
The cavity is generally cylindrical, i.e. is translationally symmetrical along the coronal-apical axis, as the case may be up to the branching into the sub-cavities. It is limited apically by an abutting portion, which in particular can include an energy director. Such an energy director can include a coronally projecting edge or tip.
Likewise the subject-matter of the invention is an implantation set, which apart from the implant also includes a sonotrode that is shaped to engage with its distal end from coronally into the cavity and to apply the mechanical oscillations as well as the pressing force.
Such a sonotrode can be coupled directly onto a device for producing the mechanical oscillations, or an intermediate part between such a device and the sonotrode can be used, for example, for deflecting the oscillations. Such an intermediate part is disclosed, for example, in WO 2007/101 362.
If condition B is fulfilled, the sonotrode in particular can likewise include a non-rotationally-symmetrical distal end with a cross-sectional shape that corresponds, for example, to the cross-sectional shape of the cavity.
A method for the patient-specific manufacture of an implant of the type described in this text is further the subject-matter of the invention. For manufacturing the implant body, in a first step, data of a patient is taken by way of measurement and is converted into a 3D model of an implant. This 3D model, as mentioned above, is subsequently adapted manually or by way of software such that a cavity or a plurality of cavities with the characteristics that are described in this text is incorporated. The dental implant body is then manufactured as a physical implementation of the 3D model that is provided with the cavity, in a computer-assisted manufacturing method. Such manufacturing methods, which are based, for example, on a computer-controlled, targeted local excitation of the manufacturing mass for the purpose of solidification, in the meanwhile are known and are not described further here.
Likewise the subject-matter of the invention is an implantation method.
Embodiment examples of the invention are explained hereinafter by way of figures. In the figures, the same reference numerals indicate the same or analogous elements. There are shown in:
For illustration purposes,
One can see that in all cases the enossal region is not undercut or is only undercut to a small extent (given roots with two or more root canals) with respect to directions along the coronal-apical axis 13. The shapes can therefore be well approximated by way of non-undercut implant shapes, which can be inserted in the apical direction by way of a non-rotating movement.
The implant body 1 is manufactured, for example, of a zirconium oxide ceramic, in particular of an yttrium-stabilised ceramic based on zirconium oxide. Generally, the teaching that is described here by way of embodiment examples, however, also applies to implant bodies of another material, for example, of another ceramic, in particular based on aluminium oxide, or of a metal, for example, titanium or a titanium alloy. As already explained beforehand, the implant body can have been optionally manufactured in a patient-specific manner by way of suitable computer-assisted (CAD/CAM) methods (by way of 3D printing in the broadest sense). In such embodiments, the material selection can be adapted in accordance with the manufacturing method and, for example, be likewise selected on the basis of ceramics or metal, wherein the price, stability and metal sensitively can serve as criteria. Suitable materials are known per se, depending on the initial situation.
A cavity 2, which is open to the coronal end, extends over almost the entire length of the implant and is delimited apically by an abutting portion 5 extends apically from the coronal end in a manner roughly parallel to an axis 13. Two exit openings 4, which lie opposite one another, are formed radially outwards from the cavity 2 towards the outer surface (lateral surface). The abutting portion 5 is slightly pointed towards the middle so that its forms an energy director.
As one can see in
Furthermore, one can see that the outer shape optionally does not taper apically to all sides in the same manner, but in a non-uniform manner so that, for example, the apical tip does not lie on the axis 13. The centre of gravity of the horizontal section surface (i.e. of the surface in the section perpendicular to the axis 13) does not therefore run in a constant manner as a function of the axial position, but the respective centre of gravity line 14 is slightly arcuate. However, the outer surface of the enossal region of the implant body forms, for example, no undercut.
A post 61 for fastening a superstructure is formed in the coronal region. The cavity 2 extends axially through the post 61. In the drawn embodiment example, a step 63 forms between the apical region and the post 61. This step can be formed roughly at the level of the gingiva, and a projection, which is yet described hereinafter and is for the compression of the gums, can yet be optionally present. Differing from that which is drawn, another in particular continuous course can be present instead of a pronounced step 63, and respective shapes are known from dental implants of single-part systems or from abutments of two-part systems.
An opening 2, which is open to the coronal end, extends almost over the complete length of the implant and is delimited apically by abutting portion 5 extends apically from the coronal end in a manner parallel to the axis 13. Two exit openings 4, which lie opposite one another, are formed radially outwards from the opening 2 towards the outer surface (lateral surface). The abutting portion 5 is slightly pointed towards the middle, so that an energy director 7 whose function is yet explained hereinafter is formed.
A sonotrode 22 with a cross section that is adapted to the cavity 2 is moreover indicated. The cross section of the sonotrode 22 is such that this can be inserted into the cavity 2 essentially without any force effort when this cavity is free. The cavity 2, for example, is cylindrical, i.e. at least in regions it has a cross section that is constant along the coronal-apical axis 13.
For the implantation, the implant is inserted into the extraction alveolus or cavity and, for example, is lightly hammered in, for example, subsequently to the extraction of the natural tooth—possibly with an additional preparation step as is yet described hereinafter—or also subsequently to the preparation of a corresponding cavity in the jawbone.
The thermoplastic element is then pressed apically against the abutting portion 5 by way of the sonotrode 20 whilst this sonotrode is subjected to mechanical oscillations, by which means the thermoplastic material of the thermoplastic element 20 in contact with the abutting portion 5 is heated until it becomes flowable and is displaced outwards through the exit openings 4 and into the structures of the bone tissue on account of the pressing pressure. Here, the shape of the abutting portion, which acts as an energy director, can have the effect of the energy absorption initially primarily taking place in contact with this, by which means the thermoplastic material is heated there most of all. Since the internal friction of the thermoplastic material is much greater when this has a higher temperature (for example, with amorphous thermoplastics when it lies above the glass transition temperature), the energy absorption also subsequently takes place predominantly at the apical end, by which means it is ensured that liquefaction takes place in the region of the exit openings 4. The interface between the sonotrode 22 and the thermoplastic elements 20 displaces continuously apically during this process, by which means the coronal regions of the cavity remain essentially free of thermoplastic material depending on the length of the thermoplastic element and after removal of the sonotrode can serve another purpose—for example, for the fastening of an abutment between the implant body and the crown or a fastening part for a prosthesis—and/or can be closed by a suitable element.
The embodiment according to
The embodiment according to
The implant body 1 coronally forms a pronounced projection that is arranged transgingivally in the implanted condition. In the region of the projection, the implant can optionally have a somewhat larger cross section than the extracted tooth. The gums are slightly compressed by way of this, which is already known per se from conventional implant systems.
The abutting portion 5 forms a pronounced, coronally pointing tip 7 that acts as an energy director and encourages the onset of the liquefaction of the apically pressed thermoplastic element when mechanical oscillations are coupled into this.
In a first step, the implant body, optionally with an already introduced thermoplastic element is positioned relative to the bone and is introduced into the extraction alveolus or another matching bone opening. This step can optionally include a knocking into the bone. As is illustrated in
A crown 81, which is subsequently placed on in a direct manner or indirectly via an abutment—possibly after a gum healing phase with an applied gingiva former—can be fastened to a post 61 and/or to the opening 2 and/or to the implant shoulder and/or to another structure of the implant body and possible also of the thermoplastic material.
By way of an implant with two root canals,
Generally and independently of whether wings of the illustrated type are present or not, in many embodiments an outer cross section of the thermoplastic element and/or of a distal end of the sonotrode is adapted to the inner cross section of the cavity - of the portion up to the abutting portion 5 or the abutting and branching portion 95.
This is illustrated in
As explained above by way of
For this purpose, concerning the embodiments with cutting edges, it can also be advantageous if no cutting edges are located coronally of the exit openings.
Firstly, it serves as the cavity for the introduction for the thermoplastic element, the cavity having the exit openings 4.
Secondly it serves for receiving a fastening post 222 of a dental abutment 220 as, for example, illustrated in
In the example of
Other connections between the cavity and the fastening post may be possible, such as positive fit connections (for example, similar to a bayonet fitting etc.) or any friction fit or adhesive bond or combinations of positive fit, friction fit and/or adhesive bonds. In the case of an adhesive bond, the implant or a set including the implant may include an according adhesive.
The abutment in addition to the fastening post 222 includes a coronal post 221 for securing a crown or prosthesis to the implant. The coronal post 221 may optionally have a non-round cross section; the same holds for the fastening post 221.
In the illustrated embodiment, the anchoring part 200 is illustrated to be a bone level anchoring part, shaped to be implanted in a manner that the coronal end is approximately flush with the outer surface of the bone tissue. In these embodiments, the abutment 220 may include a widened intermediate portion 224 between the fastening post and the coronal post, the intermediate portion being configured to reach across the gingiva in the implanted state.
The abutment may be essentially circularly symmetrical about the coronal-apical axis or may have a shape different from such symmetry, as illustrated for the intermediate region 224 as well as for the coronal post 221 in
In
To this end, the dental implant may in addition include a protection sleeve 250 as, for example, illustrated in
A protection sleeve may have a, for example, apical coupling portion cooperating with a coupling structure (for example, the thread if applicable) of the anchoring part so as to have a precisely defined position relative to the anchoring part and to be well centered. Also, the coupling portion may prevent thermoplastic material from flowing back along an outer surface of the protection sleeve. Such apical coupling portion may, for example, include outer thread structures engaging in the inner thread 208 or other suitable structures.
The protection sleeve has an inner diameter large enough for accommodating the thermoplastic element 20 and an outer diameter small enough to fit into at least a coronal part of the cavity 202 to protect those structures from getting into contact with flowable thermoplastic material, which are needed to establish the connection with the abutment. For the embodiment of
The protection sleeve (if applicable) protects the inner thread 208 from being interpenetrated by thermoplastic material of the thermoplastic element 20.
In addition or as an alternative, to protecting an inner thread, a protection sleeve may be placed to protect other structures for securing the abutment to the anchoring part, namely a conical portion, as illustrated hereinbefore, other positive-fit structures, structures to which an adhesive (cement) is to be applied, etc.
Instead of the abutment having a widened portion 224 arranged transgingivally, the anchoring part 200 may include in addition to an enossal portion 230 having the enossal outer surface, a transgingival portion 231 coronally thereof, as shown in
Often (this holds both, for the one-part implants according to
Coronally of the anti-rotation section the cavity has a conical region 214 for cooperating with a corresponding conical region 223 of the abutment as described hereinbefore, and coronally thereof it has a cylindrical receiving section 215.
The abutment 220 shown in
Various other combinations are possible, including combinations or sub-combinations of features described referring to
| Number | Date | Country | Kind |
|---|---|---|---|
| 01001/16 | Jul 2016 | CH | national |
This application is a continuation-in-part application of U.S. application Ser. No. 15/662,585 filed Jul. 28, 2017, which itself claimed priority to CH 01001/16 filed Jul. 29, 2016, both of which are expressly incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15662585 | Jul 2017 | US |
| Child | 16951476 | US |
