|Publication number||USRE38945 E1|
|Application number||US 09/667,827|
|Publication date||Jan 24, 2006|
|Filing date||Sep 22, 2000|
|Priority date||Jan 30, 1995|
|Publication number||09667827, 667827, US RE38945 E1, US RE38945E1, US-E1-RE38945, USRE38945 E1, USRE38945E1|
|Inventors||Paula S. Fried, Leonard Cooper|
|Original Assignee||Paula S. Fried|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (35), Non-Patent Citations (9), Referenced by (6), Classifications (4), Legal Events (7)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This is a continuation in part of Ser. No. 08/380,850, filed Jan. 30, 1995, now U.S. Pat. No. 5,580,246.
This invention relates generally to a dental prosthesis and more particularly to a dental prosthesis that is attached to an implant in the bone of a person's jaw.
It is now common when it is desired or necessary to replace a missing tooth or teeth, that the gum is opened and an implant is imbedded in the bone structure beneath the gum. The implant is held initially by friction in a socket formed in the bone or the implant may be threaded into the bone. The gum is then closed over the implant and heals. When a proper material is used for the implant, the bone and implant grow together by a process known as osseointegration so that after several months the implant becomes a permanent part of the bone structure in the mouth. Titanium has been an effective implant material.
Many firms manufacture complete systems of dental implants and prosthetic components for subsequent attachment to the implants. In a typical construction, the implant has an axially threaded hole at its top, that is, the proximal end, near the gum surface. After the implant has integrated with the bone, the gum of the implant is opened to expose the tapped hole. Then an abutment is attached to the tapped hole of the implant and extends to a level above the gum or substantially to the gum surface. The protruding fee end of the abutment is constructed for attachment of a prosthesis. For preventing rotation of the prosthesis, the protruding end of the abutment requires a non-round shape and a hexagonal protrusion has been widely used. The abutment also includes a central threaded hole concentric with the threaded hole of the implant and extending inward toward the jaw bone.
A false tooth or crown is provided with a hole therethrough, known in the art as a chimney, and a non-round recess in its base corresponds in shape to the protruding non-round cross section of the abutment. Thereby, the crown can be connected to the abutment and relative rotation between them is prevented so long as critical contours of the abutment and the recess in the crown are maintained.
To prevent the crown from lifting axially from the abutment, a final screw, sometimes known in the dental profession as a “gold screw”, is passed into the chimney opening and engages the tapped hole in the implant by way of the abutment so as to hold the crown axially to the abutment and to the implant. Thus, the crown cannot rotate about the abutment or implant because it is mated with the special contours on the exposed end of the abutment. The abutment is similarly mated to the proximal or outer end of the implant. The crown cannot pull away from the abutment when the gold screw has been tightened into place.
Finally, the chimney above the gold screw is filled with a composite material that hardens and is shaped as part of the crown to look like a natural tooth.
There are many variations in construction.
In many instances, the crown is attached directly to a non-round protrusion of the implant and is held directly to the implant by a gold screw without use of an intermediate abutment.
The implant is intended to be a permanent fixture in the jaw bone. The abutment and crown may be replaced if necessary due to damage or poor fit by gaining access to the screw head by way of the chimney, and backing off the screw so that the crown and abutment, if used, can be separated from the implant. Thus, repairs may be made of an abutment and crown with relative convenience.
Whereas dental implantations go back to the days of the Pharaohs in Egypt, use of titanium metal implants that integrate with the bone itself, is a recent development over the last 25 to 30 years. Data so far available on the service life of such implants, indicate that most implants can be expected to have a long service life without complications of the implant itself. However, in a significant percentage of implants, a problem arises because titanium is a relatively soft metal. An unacceptable degree of looseness often develops between the implant and the adjacent abutment or crown whereby there is relative rotation between the implant and the attached elements. This rotational latitude occurs when the contours of the protrusion at the proximal end of the implant become worn as a result of lateral forces applied on the protrusion. Such forces are transmitted from the crown as the crown interacts with adjacent teeth, and perhaps bones, during the course of chewing, biting and nervous grinding (bruxism). Tremendous rotational forces are known to act on the crown. Once there is some degree of freedom for rotation of the crown relative to the implant, the non-rounded contours of the implant protrusion tend more and more toward roundness, and permit more and more rotation. In time, the connection between the implant and the abutment and crown connected thereto does not prevent rotation and is unacceptable.
In these types of failure, for example, where the original protrusion on the implant was hexagonal in shape, it has been found that the corners of the hexagonal shape have been rounded to such a degree that it is not possible to attach a new crown or abutment and prevent rotation relative to the implant.
As stated, this type of rounding on the implant protrusion occurs during normal use of the prosthesis in biting and chewing. Also, the contours of the implant protrusion may become distorted, especially unfavorably rounded or stripped, during the process of threading the implant into the jaw bone. This occurs because the implant protrusion is the means by which the driving tool engages the implant. Therefore, when hard bone is encountered, it is possible that an implant may be damaged beyond usefulness by an ill fitting socket type wrench that engages the outer surfaces of the protrusion and is used to drive-in the implant.
This situation, though costly, is not catastrophic when initially inserting an implant in that the damaged implant may be removed and a new one may be inserted. Unfortunately, after the implant has been joined to the jaw bone by osseointegration, and after years of this condition, it is extremely difficult, costly, and the cause of considerable suffering to the patient, to attempt to remove a damaged implant and replace it with another.
What are needed are a method to rehabilitate in the mouth a damaged implant that no longer holds the crown effectively against rotation, and an improved implant that better resists rotation of an attached abutment and/or crown and thus has an extended service life.
Accordingly, it is an object of the invention to provide a method for rehabilitating the proximal end of an implant so as to prevent relative rotation of abutment or crown elements after the initial attachment means has failed.
Another object of the invention is to provide an improved dental implant that reduces the hazards of damage to the implant attachment protrusion during installation and of damage due to crown rotation during normal usage over the life of the prosthesis.
Yet another object of the invention is to reduce the occasions when an implant that has osseointegrated with the jaw bone needs removal in its entirety.
In a method to rehabilitate or replace an implant having a damaged proximal protrusion, such that there is unacceptable rotation between the implant and an attached abutment and/or crown, a jig is slipped over the remaining implant protrusion after removal of the crown and abutment. Guided by the jig, a burr forms radial slots, or other indentations, in the outer surface of the implant adjacent to the protrusion. The slots or other indentations may extend into the implant protrusion. A new abutment (and/or crown) is prepared by techniques that are a modification of casing techniques well known in the dental arts. The bottom surface of the prosthetic device that engages the implant precisely engages the newly-added radial slots or indentations on the implant such that when the final screw is tightened into place, rotation between the implant and the attachments is prevented.
Modified analog implants, copings, and abutments facilitate the method.
Further, an improved implant in accordance with the invention has a proximal protrusion that is generally square in cross section and further includes radial slots for use in threading the implant into the jaw bone. Thereby, no forces need be applied directly to the protrusion's external surfaces when inserting the implant for subsequent osseointegration. In this way, the surfaces of the protrusion that are used to maintain the abutment and/or crown against rotation relative to the implant are not subject to inadvertent damage during installation of the implant in the jaw bone. Further, the rotation resisting surfaces of the squared protrusion are broad and generally continuous and adjacent surfaces meet at 90° angles, or less. Forces tending to rotate the crown have little effect on the holding power of the proximal protrusion even should the edges of the protrusion be removed or become rounded.
In accordance with the invention, radial slots may be formed into the protrusion itself or extend radially from the base of the protrusion. Slots may be provided in different radial directions.
Further, the slots may be omitted whereby the implant, if threaded into the jaw bone, is driven by a tool applied to the protrusion. Many cross sections are available for the protrusion to provide a non-round shape. These cross sections include regular and nonregular convex and nonconvex polygons, rounded shapes, and fluted surfaces.
The invention accordingly comprises the several steps in the relation of one or more of such steps with respect to each of the others to effect rehabilitation of an implant, and the apparatus embodying features of construction, combinations of elements and arrangement of parts which are adapted to effect extended service life for such implants, all as exemplified in the following detailed disclosure, and the scope of the invention will be indicated in the claims.
For a fuller understanding of the invention, reference is had to the following description taken in connection with the accompanying drawings, in which:
FIG 10a and 10b are a top and side elevation, in section, of another implant of the invention;
The present invention is concerned with the problem of rotation of a crown, or an abutment and crown, relative to a dental implant to which the abutment and crown are attached. In many applications, the abutment is omitted and a crown attaches directly to the implant. In every instance, the inherent problem of relative rotation is substantially similar. Accordingly, any description that includes an abutment, or any description that omits use of an abutment, is also applicable to the other construction.
A hexagonal boss 42 on the implant 12 protrudes above a surface 44 of a flange 45 of the implant 12. The base 46 of the crown 22 includes a hexagonal socket 48, whereby the crown 22 can be removably connected to the implant 12 with the implant boss 42 engaged in the hexagonal socket 48 of the crown 22. Thereby, rotation of the crown 22 about the longitudinal axis 49 of the implant 12 is prevented by the hexagonal cross-section.
Threads 32 of a screw 34 engage the tapped hole 20 until a bevel surface 36 on the screw bead 38 engages a shoulder 40 on the crown 22. Tightening the screw 34 into the threaded hole 20 of the implant 12 draws the crown 22 into a rigid axial connection with the implant 12 and consequently with the bony structure 14, 16 of the jaw.
In attaching the crown 22, the screw 34 is tightened by means of an Allen-head type tool that engages the hexagonal socket 50 in the screw head 38. Then the chimney 30 is filled with a filler material, known in the dental arts, and the exposed surface of the filter material is contoured to match the remainder of the crown.
The implant 12 may be screwed into the jaw bone or may be pressed into a prepared socket. When a titanium implant 12 is used, as is the current practice, it is anticipated that an osseointegration process will bind the implant 12 permanently into the jaw after a period lasting three to six months. Then, the crown 22 is prepared to custom fit the integrated implant within the space available between adjacent teeth. Frequently, a gum shaping device or healing cap (not shown) is threaded into the tapped hole 20 and maintained in place while the gum heals after the initial implantation. When screwed into the bone, the implant 12 is driven by attachment of an Allen-head type tool onto the protruding boss 42. To reduce any hazard of damaging the surfaces of the protrusion 42 while tapping (threading) the socket in the bone, an analog implant (not shown) of material stronger that titanium, e.g. stainless steel, may be used. After the socket is tapped, the actual implant 12 is threaded into the prepared opening. Once the final setting is made, hopefully, the implant will never need removal.
Whereas an attached crown, which is damaged, can be replaced with relative ease, there is no purpose to such a procedure unless steps are taken to prevent future relative rotation between the crown 22 and the implant 12.
By a rehabilitation method in accordance with the invention, the proximal end of the implant 12 is modified in vivo by the addition of slots 56 (
The lower or bottom surface
Next will be described methods, in accordance with the invention, for rehabilitating an implant 12 in the mouth to provide the constructions illustrated in
First, the proximal end of the implant 12 is exposed by removal of the crown 22 and an abutment, if one was used intermediate the implant and the crown. As a result, the protrusion or boss 42 and the surface 44 on the implant are exposed to view (FIG. 3).
These external elements are removed after exposing and backing out the screw 34 via the chimney 30. Then a notching jig 64 (
The notching jig 64 has a long stem with a longitudinal opening 70 through which a threaded screw (not shown) is inserted so as to engage the central opening 20 in the implant 12. Thus, the jig 64 is axially fixed into position on the implant 12 even though the boss 42 is worn. Guide holes 72 extend from a rear shoulder 74 on the jig 64 to the interface surface 66. Four guide holes 72 are illustrated; in practice, two guide holes are sufficient when two slots 56 are to be formed in the implant surface 44.
With the notching jig 64 in place on the implant 12, the dental practitioner runs a rotating burr through the guide holes 72, in turn, and forms indentations 56 into the upper surface 44 on the flange 45 of the implant 12. A stop on the burr or shoulders (not shown) within the guide holes 72 limit the depth of the indentation 56 formed in the surface 44 of the modified implant 12′. Thus, a configuration as shown in
Alternatively, the guide holes 72 may be radially oriented ovals (not shown), extending inwardly toward the opening 20 so that the burr may provide extended slots in the implant 12 that cut into the protrusion 42. These elongated slots, the extensions indicated in
In another embodiment of the method for repair, a notching jig may provide slots only into the boss 42 and not in the flange surface 44.
Repair of an implant already imbedded in the jaw bone and osseointegrated has been described above, describing the indents formed into the implant as “slots”. It should be understood that indentations having contours other than the radial slots illustrated in
It is now necessary that the abutment and crown which ultimately attach to the modified implant 12′ be made to precisely mate with the slots 56 (or other indentations) formed on the surface 44 of the implant. For the sake of the following description of repair procedures, it is assumed that no separate abutment element is used intermediate the implant and the crown in the completed prosthesis. Further, generally rectangular slots are described; the procedures also apply to indentations of other shapes.
How to make a crown for attachment to an osseointegrated implant in the jaw is well known in the art of dental implants. The same basic procedures are followed in making a crown for the now-modified dental implant 12′, which is still embedded in the jaw bone, however with slight changes in the elements that are used to accommodate the slots now formed in the flange surface 44 of the implant 12′. The finished crown must have protrusions on its lower inner surface that interface with the implant to complete the prosthesis.
Therefore, conventional fabrication techniques using a direct pick up impression or an indirect impression would readily be implemented by those skilled in the implantation art without further explanation. However, a brief description (and flow diagram
In a direct pickup technique, after notches or slots 56 are prepared on the implant 12′ with the notching jig 64, as described above, a direct impression of the modified top of the implant 12′ is made by customizing a resin UCLA-type abutment, using a well-known auto-polymerizing resin.
The customized abutment 76 is attached to the implant 12′ by a guide pin (not shown) that passes through the longitudinal opening 82 in the stem 84 of the abutment 76 and engages the tapped opening 20 in the implant 12′. Then the impression material is applied to fill the spaces between the abutment 76 and the implant surface 44. After the impression material has hardened, the guide pin is unscrewed from the implant 12′ and the abutment 76 is removed. Covering the end 86 of the abutment 76 that opposed the implant 12′, protrusions 62 are present exactly corresponding to the slots 56 newly formed on the implant 12′.
Then, the customized abutment impression (not shown) is cast into a strong, rigid material e.g. metal. The resultant metal abutment is placed over the implant 12′ in the jaw, and is secured in place with a guide pin that engages the central opening 20 of the implant 12′ by passing through a central opening in the metal abutment that corresponds to the opening 82 that was in the customized UCLA-type abutment 76. The protrusions 62 are seated in the implant slots 56.
Then a pick-up impression is made in the mouth in the conventional manner, that is, a window is cut in the top of an impression tray; the tray is filled with impression material and some of this material is positioned around the abutment. Then the filled impression tray is placed over the implant 12′ and metal abutment with the guide pin protruding through the impression material and from the upper surface of the tray. After the impression material has hardened in the tray, the guide pin is unscrewed and the impression tray with the metal abutment now embedded in the impression, is removed from the mouth. The protrusions 62 on the face of the metal abutment are visible in the impression.
A modified implant analog (stainless steel) having slots that correspond with the slots 56 which were formed using the jig 64, is positioned on the abutment with the slots on the implant analog receiving therein the protrusions 62 on the metal abutment, which was embedded in the impression. The implant analog is fixed to the abutment with a guide pin, and the assembly is poured in stone, that is, a rigid modeling material. After hardening, the guide pin is removed, and the impression containing the abutment is separated from the stone.
The stone model now positively replicates the portion of the jaw including the implant 12′. The model includes the analog implant with slots having the exact same dimensions and orientation as those slots 56 in the actual implant 12′ in the jaw bone of the patient.
The metal abutment is now removed from the earlier impression material. The metal abutment was made with protrusions 62 that exactly mate with the analog implant. From this state, a crown is fabricated by well known procedures. The crown incorporates the metal abutment, thus assuring a perfect fit for the crown in the mouth.
Rotation of the crown relative to the modified implant 12′ is prevented by engagement of the protrusions 62 from the abutment with the slots 56 in the exposed surface 44 of the implant 12′.
In a conventional indirect impression technique, slots 56 (
Then an impression tray with a window cut out of the top is placed over the implant and surrounding portion of the jaw so that the guide pin protrudes. The tray is filled with impression material in a conventional manner. After the impression material has set, the guide pin is unscrewed and the impression is removed from the mouth. An implant analog (e.g. stainless steel) is then abutted with the coping in the impression, with slots being provided on the implant analog to mate with the protrusions, which are extending from the surface of the impression coping. After the implant analog abuts the coping in the impression, the analog and coping are secured together with a guide pin, and a model is poured in stone. The stone model replicates, at least partially, the jaw of the person, however, with the proximal end of the implant analog exposed to view, including its slots in the proper orientation. Then a crown is fabricated by conventional procedures. New materials, namely nylon, gold and aluminum oxide (Al2O3) may be used in fabricating the crown on the stone model in this technique.
In the above methods, it has been assumed that the drill jig 64 is used in modifying the implant 12 in the jaw. When this is done, the hardware, namely the copings and analog implants, are pre-manufactured, off-the-shelf items with protrusions and slots that will fit or match the slots that were made in the actual implant in the jaw bone.
However, many practitioners will prefer not to use such a jig 64 and will instead produce a variety of indentations of their own preference on the surface 44 of the implant 12 in the mouth. In such a situation, pre-manufactured implant analogs and pre-manufactured copings with the proper patterns of slots and protrusions, as required, will not be available off-the-shelf.
Therefore, to practice the above procedures, it is necessary to first make a direct pick up from the implant 12′ in the mouth, using a customized UCLA-type abutment 76 (
Next, an embodiment of an implant in accordance with the invention is discussed, which will reduce the hazards of stripped and damaged boss surfaces that would in time prevent proper mating with an abutment and/or crown. The same reference numerals are used in the description of the improved implants where elements correspond to those of
In an implant 90 of
Each of the sides 96 of the boss 92 have a greater continuous length as viewed in
The boss 92 is bevelled (similar to
Additionally, the slots 94 are provided for the purpose of screwing the implant into the bone. The bone is frequently pretapped using a dummy (analog) implant that is made of tougher metal or plastic than the titanium implant itself. The tool which is used for threading the implant 90 into the bone of a patient (not shown) is constructed such that it rotates the implant 90 by tool engagement with the slots 94 and not because of any driving engagement with the sides 96 of the boss 92. Thus, the surfaces of the boss 92 do not become damaged by the insertion tool upon the initial installation of the implant into the jaw bone, and the contours of the boss 92 are preserved for accurate and effective mating with the abutment and/or crown.
To further assure the fixed relative position between the implant and that which is externally attached to it, the abutment or crown that interfaces with the implant 90 may be made with protrusions that engage in the slots 94 at the interface.
It should also be understood that because of the increased strength of the square boss 92, the boss may be used when threading the implant into the jaw bone, and the slots 94 may be omitted. In such a use of the boss 92, the likelihood of serious damage to its surfaces, so as to render its attachment to an abutment and/or crown rotationally unacceptable, is much less than with hexagonal boss 42 of the prior art.
The implant 98 of
The slot 94′ may penetrate in depth into the upper surface 100 of the boss 92, as illustrated with the solid lines in FIG. 10a. On the other hand, the slot depth may be extended (not shown) substantially, even into the flange 45, that is, below the surface 44 of the flange 45. In any event, the slot ends 102 do not extend through to the outer periphery 60 of the flange 45 to reduce hazards of bacterial activity. It is also desirable for similar reasons that the slots do not open into the tapped hole 20.
For the purpose of increased strength of the boss 92, if needed, it is possible in manufacture to enlarge the size of the generally square shape and possible lose the perpendicular intersections as indicated by the broken lines 104 in FIG. 10a. (In all constructions, there is a trade-off between the implant strength and the strength of the attached device.)
Another alternative embodiment (
In installing such an implant 117 into the jaw bone, it is preferable that a tool that engages the slots 121 is used without engagement with the protrusions 119 for driving purposes. However, it should be understood that the bosses 119 can be used in driving the implant 117 into the jaw bone and a driving tool can be made for that method. Further, both the slots and the bosses may be used when driving the implant into the jaw bone when a properly mating tool is provided. The implant in
In each embodiment, it is intended that the implant be threaded into the jaw bone using only the slots in the proximal implant end. Nevertheless, it is recognized that the boss outlines, whether square, elongated rectangular, triangular, etc., because of their cross sectional bulk and long sides with reduced intersection angles present considerably more resistance to deformation than the prior art hexagonal cross section of the boss 42 (FIGS. 1-3).
Further, it should be understood that the hexagonal boss, or any shape of the prior art, may be retained (
Whereas the figures have illustrated bosses having different polygonal cross sections that are defined by straight lines and crisp intersections of those lines, it should be understood that rounded and bevelled edges, are intended to fall within the scope of the invention. Additionally, any generally axially oriented side surface of a boss may include a bulge or concavity so long as the basic polygonal shape is retained. For examples,
Additionally, in the discussions above, the implants are described as having a central tapped opening 20. However, implants are known in the art wherein the central opening is not tapped and may have a non-round cross-section. In such cases, the crown assembly has a post that extends into the central opening of the implant and an adhesive is used to prevent axial motion of the crown relative to the implant after the adhesive has set. A non-round boss as described above in accordance with the invention prevents the rotation of the crown relative to the implant.
Further, the use of screws that pass through the jaw bone and the implant, and in some instances through the post on the crown that is received in a central opening of an implant, is known in the art, for example, U.S. Pat. No. 5,542,847. All such means for maintaining the axial relationship between the crown and the implant when combined with the bosses, slots etc. in accordance with the invention, are intended to fall within the scope of the invention.
Generically speaking, the cross-sectional shape of the boss in accordance with the invention is made non-round such that should the linear edges extending from the surface 44 become rounded there would remain a distinct non-round cross section for the boss. The hexagonal shape of the prior art and any regular polygon cross section having five, six or more regular sides is vulnerable to circular rounding as vertical edges become worn.
On the other hand, convex polygons as shown, for example, in
Further, a generally circular boss cross section can be given holding power against turning by an abutment or crown by use of axially oriented flutes that are formed internally, or externally as teeth. Basic shapes, such as a triangular or square cross section boss may also have supplemental internal or external flutes. Regular hexagonally shaped bosses, by addition of internal and/or external flutes or other formations, maintain a non-round cross section when the axial edges are rounded.
Bosses with cross sections that are convex polygons are illustrated in
Nonconvex polygons are illustrated in
Each of the polygons can be altered such that sides become concave or convex curves and corners can be rounded so long as the resultant shape retains the desired non-round characteristic that resist turning and wear by an attached prosthesis element. For example, the boss of
In each of the embodiments 19a-m, indentations (not shown) may be provided into the surface 44 for use in threading an implant into the jaw bone, as discussed above.
For the purposes of the descriptions above and the claims that follow, the definitions of different polygons and their features are based upon the school text: Addison-Wesley Geometry, by Stanley R. Clemens, Phares G. O'Daffer, Thomas J. Cooney, John A. Dossey; Addison-Wesley Publishing Co., Inc. Menlo Park, Calif. (1994). In particular, pages 135-140 and later pages, are a source of definitions.
A convex polygon is defined as one in which all diagonals are interior. A nonconvex polygon is one where not all diagonals are interior. A regular polygon is equiangular and equilateral. A trapezoid is a quadrilateral polygon with one pair of parallel sides. A polygon has n sides with the sides meeting at vertices.
Thus, methods for repairing damaged implants in the mouth, and improved implants have been presented. All of those devices that engage the repaired implant, are provided with recesses and protrusions, as required. However, a crown, for example, having a recess with a square cross section so as to match an implant of
It is contemplated that in practicing the methods, a kit of parts will be purchased from a dental supplier. The kit for those practitioners using preferred methods includes a notching jig 64 and an appropriate burr (not shown) to fit the guide holes 72. Also in the kit may be an implant analog having preformed slots 56 on its proximal end, and an impression coping having protrusions 62 on its lower end. A modified UCLA-type abutment with dove-tail teeth may also be in such a kit, although it could be purchased separately. A different kit for a practitioner who prefers not to use the notching jig may instead include a UCLA-type abutment and a modified implant analog that has no flange 45.
It should also be understood that a reversal of features is intended to fall within the inventions scope. Thus any boss cross-section which has been described as protruding from the flange surface 44 may also be formed (and viewed in the Figures) as a recess in the surface 44. In such a construction the mating crown or abutment is fabricated with a correspondingly shaped protrusion (or protrusions) that seat(s) in the recess (or recesses).
It will thus be seen that the objects set forth above, among those made apparent from the preceding description, made in carrying out the above methods and in the articles set forth without departing from the spirit and scope of the invention, it is intended that all matter contained in the above description and shown in the accompanying drawings shall be interpreted as illustrative and not in a limiting sense.
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|3||Branemark System Streamline Simplicity Defined, Nobel Biocare, Inc., Product Catalog (2000).|
|4||Branemark System US Product Catalog 6<SUP>th </SUP>Edition, Nobel Biocare, Inc., Product Catalog (Oct. 2000).|
|5||Branemark System US Product Catalog 6th Edition, Nobel Biocare, Inc., Product Catalog (Oct. 2000).|
|6||Primary Stability is Essential for a Good Life, Nobel Biocare, Inc., Product Catalog (1999).|
|7||Small Diameter Implants Solutions for Restricted Spaces, 3i, Inc., Product Catalog (1997).|
|8||Univeral Fixture Mk III Featuring Stargrip(TM), Nobel Biocare, Inc., Product Catalog (1999).|
|9||Univeral Fixture Mk III Featuring Stargrip™, Nobel Biocare, Inc., Product Catalog (1999).|
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|U.S. Classification||433/172, 433/173|
|Jan 19, 2001||AS||Assignment|
Owner name: FRIED, PAULA S., NEW YORK
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:FRIED, PAULA S.;COOPER, LEONARD;REEL/FRAME:011458/0629;SIGNING DATES FROM 20000814 TO 20000822
|Mar 20, 2006||FPAY||Fee payment|
Year of fee payment: 8
|Sep 25, 2009||FPAY||Fee payment|
Year of fee payment: 12
|Dec 1, 2009||CC||Certificate of correction|
|Dec 15, 2009||AS||Assignment|
Owner name: SMALL, PAULA N., NEW YORK
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:MAROTTA, LEONARD;REEL/FRAME:023652/0834
Effective date: 20091119
|Dec 22, 2009||CC||Certificate of correction|
|Apr 19, 2011||CC||Certificate of correction|