Method for forming a dental prosthesis

Information

  • Patent Grant
  • 7632095
  • Patent Number
    7,632,095
  • Date Filed
    Monday, August 13, 2007
    17 years ago
  • Date Issued
    Tuesday, December 15, 2009
    15 years ago
Abstract
A method of creating a provisional dental prosthesis on an implant placed in bone retains a conical abutment to the implant. A first intermediate component secures to the conical abutment. A second intermediate component attaches to the first intermediate component. The second intermediate component comprises a polymeric material. A prosthetic template is placed over the second intermediate component. The prosthetic template is filled with a hardenable material. After the prosthetic template is filled, the process removes the prosthetic template with the second intermediate component within the hardenable material. A provisional prosthesis forms from the hardenable material, the provisional prosthesis contains the second intermediate component. The provisional prosthesis connect to the first intermediate component by affixing the second intermediate component to the first intermediate component.
Description
FIELD OF INVENTION

The present invention relates to a method of forming a dental prosthesis. More particularly, a method of forming a provisional as well as a permanent prosthesis to be applied to at least one or two dental implants is provided.


BACKGROUND OF THE INVENTION

The dental restoration of a partially or wholly endentulous patient with artificial dentition may be a lengthy process. Some patients undergo a two stage procedure, wherein the first stage entails implanting an implant in a bone for integration. A period of time is allowed for the patient to heal, and for the implant to osseointegrate with the bone. After this period of time, the second stage involves attaching prosthetic components to the implant. These prosthetic components may include healing components to allow gingival tissue to acquire a shape that mimics a natural gingival tissue shape, or the prosthetic components may include restoration components, such as, for example, an abutment and a crown.


Recently, some patients have been undergoing single-stage implant procedures in which a practitioner places an implant and attaches prosthetic components during the same office visit. Often times a pre-made provisional prosthesis will be placed on a patient while a permanent prosthesis is being developed. Many pre-made provisional prosthesis have a shape that is not specific to that patient, but the provisional prosthesis simply replicates a typical shape of a set of teeth. One drawback associated with such a pre-made provisional prosthesis is attaching a pre-made provisional prosthesis to the implant, as implants may not be placed exactly in a planned location, attaching locations on the pre-made provisional prosthesis may not align with the placed implants. Thus, alterations may be required to allow the pre-made provisional prosthesis to mount to the implants. Thus, a need exists for a method of forming a patient specific provisional dental prosthesis.


SUMMARY OF THE INVENTION

According to one process, a method of creating a provisional dental prosthesis on an implant placed in bone retains a conical abutment to the implant. A first intermediate component secures to the conical abutment. A second intermediate component attaches to the first intermediate component. The second intermediate component comprises a polymeric material. A prosthetic template is placed over the second intermediate component. The prosthetic template is filled with a hardenable material. After the prosthetic template is filled, the process removes the prosthetic template with the second intermediate component within the hardenable material. A provisional prosthesis forms from the hardenable material, the provisional prosthesis contains the second intermediate component. The provisional prosthesis connects to the first intermediate component by affixing the second intermediate component to the first intermediate component.


According to another process, a method of forming a dental prosthesis on a plurality of implants placed in bone attaches a conical abutment to each of the plurality of implants. A metallic first intermediate component is secured to each of the conical abutments. A polymeric second intermediate component is applied to each of the metallic first intermediate components via a snap-fit. The method places a provisional prosthetic template over the second intermediate components. The provisional prosthetic template forms an inner cavity that generally replicates shapes of teeth replaced by the provisional prosthesis. The provisional prosthetic template fills with a hardenable acrylic material. The method removes the provisional prosthetic template with the polymeric second intermediate components from the mouth. A provisional prosthesis forms from the hardenable acrylic material, the provisional prosthesis containing the polymeric second intermediate components. The provisional prosthesis connects to the metallic first intermediate components by placing the polymeric second intermediate components on the metallic first intermediate components. The method creates a permanent prosthesis. The provisional prosthesis and the metallic first intermediate components are removed after the creation of the permanent prosthesis. The permanent prosthesis attaches to the conical abutments.


According to a further process, a method forms a provisional dental prosthesis on a plurality of implants placed in bone. The implants have abutments attached thereto. The method includes securing a first intermediate component to each of the abutments. A polymeric second intermediate component attaches to each of the first intermediate components. A provisional prosthetic template is placed over the second intermediate components. The provisional prosthetic template forms an inner cavity that generally replicates the shape of the provisional prosthesis. The method fills the provisional prosthetic template with a hardenable acrylic material to form a provisional prosthesis. The provisional proshetic template is removed.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 includes side views of straight conical abutments and angled conical abutments for attachment to an implant;



FIG. 2A is a front exploded view of a first intermediate component and a second intermediate component for use with the conical abutment of FIG. 1;



FIGS.2B and 2C are side cross-sectional views of the first intermediate component and the second intermediate component of FIG. 2A;



FIG. 3 is an isometric view of a patient's mouth with implants and conical abutments attached;



FIG. 4 is an isometric view of the patient's mouth of FIG. 3 with first intermediate components attached over the conical abutments;



FIG. 5 is an isometric view of the patient's mouth of FIG. 4 with second intermediate components attached over the first intermediate components;



FIG. 6 is an isometric view of the patient's mouth of FIG. 5 with a prosthetic template placed over the second intermediate components;



FIG. 7 is an isometric view of a provisional prosthesis created according to one method; and



FIG. 8 is an isometric view of the patient's mouth with the provisional prosthesis attached.





While the invention is susceptible to various modifications and alternative forms, specific embodiments thereof have been shown by way of example in the drawings and will herein be described in detail. It should be understood, however, that it is not intended to limit the invention to the particular forms disclosed but, on the contrary, the intention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the appended claims.


DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS

As shown in FIG. 1, a dental abutment assembly 10 comprises a dental abutment 12 and an abutment screw 14. The dental abutment assembly 10 is used with a dental implant (not shown) that is placed within bone of a patient. The abutment 12 shown in FIG. I is a conical type abutment. That is, the abutment 12 has a region with a generally conical shape. The abutment 12 is retained to the implant by the abutment screw 14 to form a dental implant assembly. The abutment 12 is connected to the implant after the implant is placed within the bone of the patient via the abutment screw 14. As will be described in more detail below, the abutment 12 or the abutment screw 14 includes a threaded bore 15 for retaining the intermediate components described below in FIG. 2.


While the conical abutment 12 illustrated in FIG. 1 is a generally straight conical abutment, it is contemplated that an angled conical abutment may be used. FIG. 1 also shows two conical abutments 12a and 12b having a known angle (e.g., 15° or 25°) relative to the central axis of the underlying implant. The head of the screw 14 in the angled abutments is positioned within a recess in the body of the abutment 12 and, therefore, is not shown.


Turning next to FIGS. 2A, 2B, and 2C, a provisional component assembly 16 comprises a first intermediate component 18 and a second intermediate component 20. The first intermediate component 18 is generally hollow, allowing the first intermediate component 18 to be placed over the abutment 12 once the abutment 12 is mounted to the implant. The first intermediate component 18 has a connecting region 22 and a supporting region 28. The connecting region 22 has a bearing surface 24 adapted to contact the abutment 12. The connecting region 22 additionally has a shoulder surface 25. A sidewall 26 connects the support surface 24 to the shoulder surface 25. A retention groove 27 is located along the outer surface of the first intermediate component 18. As shown, the retention groove 27 is located directly above the shoulder surface 25.


The supporting region 28 of the first intermediate component 18 is adapted to support the second intermediate component 20. As shown in FIG. 2, it is contemplated that the supporting region 28 may have a plurality of ribs 29a-29c formed in a periphery of the supporting region 28 of the first intermediate component 18. The plurality of ribs 29a-29c generally do not extend into the hollow region of the first intermediate component 18.


It is contemplated that the first intermediate component 18 comprises a metallic material. According to one embodiment, the first intermediate component 18 comprises titanium. According to another embodiment, the first intermediate component 18 comprises a titanium alloy.


A top section 30 of the first intermediate component 18 is adapted to allow a screw 150 (FIG. 2B and FIG. 4) to pass through a portion of the internal through-bore to secure the first intermediate component 18 to the abutment 12. The threads of the screw 150 may attach to a threaded bore 15 in the abutment 12 or to a threaded bore 15 in a head of a screw holding the abutment 12 to the implant, which are shown in FIG. 1. The screw 150 used to retain the first intermediate component 18 to the abutment 12 may be press fit into the first intermediate component 18 prior to the practitioner placing the first intermediate component 18 in contact with the abutment 12. It is additionally contemplated that the first intermediate component 18 may have an integral screw section, thus, eliminating the need for a separate screw (e.g., screw 150) to secure the first intermediate component to the abutment 12.


The second intermediate component 20 has an internal bore 32 with a generally conical shape that is generally complimentary to the shape of the periphery of the first intermediate component 18. The generally complimentary shape of the internal bore 32 of the second intermediate component 20 allows the secondary intermediate component 20 to be placed over the first intermediate component 18.


The second intermediate component 20 is generally a cap to be placed over the first intermediate component 18. It is contemplated that the second intermediate component 20 and the first intermediate component 18 form a press-fit, or snap-fit, therebetween. In the illustrated embodiment, a retention structure 37 within the internal bore 32 of the second intermediate component 20 contacts the retention groove 27 of the first intermediate component 18 just above the shoulder surface 25. As such, the diameter of the internal bore 32 at the retention structure 37 is sized to form a snap-fit engagement with the retention groove 27.


As shown in FIG. 2, the second intermediate component 20 has a top surface 34. The top surface 34 is a continuous surface, preventing material from entering the cavity between the second intermediate component 20 and the first intermediate component 18.


The second intermediate component 20 may have a plurality of ribs 36a-36d formed in a periphery of the second intermediate component 20. The plurality of ribs 36a-36d generally do not extend into the internal bore 32 of the second intermediate component 20.


The second intermediate component 20 preferably comprises a polymeric material. One particular polymeric material well suited for use in the second intermediate component 20 is Polyetheretherketon (“PEEK”). However, it is contemplated that a variety of other non-metallic materials may be used in forming the second intermediate component 20. For example, the second intermediate component 20 could be made of multiple materials, such as a polymeric main piece with a metallic insert to create the retention structure 37 to fit within the retention groove 27 of the first intermediate component 18. Furthermore, the second intermediate component 20 may be metallic with a polymeric or elastomeric insert, such as an O-ring, to create the retention structure 37 to fit within the retention groove 27 of the first intermediate component 18.


Turning next to FIGS. 3-8, a method of forming a provisional prosthesis will be described. As shown in FIG. 3, a patient's mouth 100 is shown containing a plurality of dental implants (not shown) having a plurality of abutments 112a-112f attached to the implants. The abutments 112a-112f are generally identical to the abutment 12 previously described relative to FIG. 1. The abutments 112a-112f are secured to the implants via a screw (not shown). The abutments 112a-112f each have a threaded section 113a-113f located at an end of the abutments 112a-112f opposite the implants. Once the abutments 112a-112f are attached to the implants, a plurality of first intermediate components 118a-118f may be attached.



FIG. 4 shows that the plurality of first intermediate components 118a-118f have been attached to each of the respective abutments 112a-112f. The first intermediate components 118a-118f are secured to the respective abutments 112a-112f via respective connecting screws 150a-150f. The connecting screws 150a-150f enter the first intermediate component at the top section 30 previously described in connection with FIG. 2. The screws 150a-150f interact with the threaded sections 113a-113f (FIG. 3) located at the end of the abutments 112a-112f opposite the implants.


As shown in FIG. 5, a plurality of second intermediate components 120a-120f are placed over each of the plurality of first intermediate components 118a-118f. As previously described, the second intermediate components 120a-120f may initially be retained on the respective first intermediate components 118a-118f via a snap-fit. It is also contemplated that a press-fit may secure the second intermediate components 120a-120f to the first intermediate components.


After the second intermediate components 120a-120f are attached to the first intermediate components 118a-118f, a prosthetic template 160 is placed into the patient's mouth 100, as shown in FIG. 6. The prosthetic template 160 surrounds the second intermediate components 120a-120f. The prosthetic template 160 may contain a plurality of generally tooth shaped cavities, including tooth shaped cavities 160a-160d for each type of tooth in the patient. For example, generally tooth shaped cavity 160a corresponds to an incisor type tooth, generally tooth shaped cavity 160b corresponds to a canine type tooth, generally tooth shaped cavity 160c corresponds to a bicuspid type tooth, and generally tooth shaped cavity 160d corresponds to a molar type tooth. It is contemplated that a tooth shaped cavity for each tooth being replaced by the prosthesis is included in the prosthetic template 160.


The practitioner may have a number of prosthetic templates 160 to choose from. The various templates may vary in size and tooth shape to allow a practitioner to select a prosthetic template that provides an aesthetically pleasing provisional prosthesis for a particular patient.


The tooth shaped cavities of the prosthetic template 160 may be patient specific. For example, a stone model of the patient's mouth may be created in a dental laboratory that includes prosthetic teeth. An impression may be taken of the stone model. The impression will have generally the same shape as a prosthetic template. The prosthetic template may then be created from the impression. It is further contemplated that the prosthetic template may be made directly by taking an impression of the stone model of the patient's mouth.


It is additionally contemplated that the shape of the tooth shaped cavities of the prosthetic template may represent idealized shapes of teeth to be replaced within a patient. The idealized shapes of teeth representing a typical shape for a tooth located within a portion of the mouth containing the prosthesis.


Once the prosthetic template 160 is placed into the patient's mouth, the prosthetic template 160 is filled with a hardenable material. The hardenable material is typically a polymeric material. One example of a polymeric hardenable material suitable for use is acrylic. The hardenable material surrounds the second intermediate components 120a-120f. Ribs on second intermediate components, such as ribs 36a-36d shown in FIG. 2, allow the hardenable material to better capture the second intermediate components 120a-120f as the hardenable material hardens. Once the hardenable material has fully hardened, the prosthetic template 160 is removed from the patient's mouth. The removal of the prosthetic template 160 additionally removes the second intermediate components 120a-120f from the first intermediate components 118a-118f. The second intermediate components 120a-120f are secured within the hardenable material within the prosthetic template 160. The hardened material is removed from the prosthetic template 160, thus forming a provisional prosthesis 170.



FIG. 7 shows a provisional prosthesis 170 formed within the prosthetic template 160. The provisional prosthesis contains the plurality of second intermediate components 120a-120f. The provisional prosthesis 170 may undergo additional processing steps prior to use in the patient, such as trimming and polishing, after being removed from the prosthetic template 160. The provisional prosthesis 170 has tooth shapes 170a-170d corresponding to the respective tooth shaped cavities 160a-160d found within the prosthetic template 160.


Once the provisional prosthesis 170 is fully prepared, it may be connected to the first intermediate components 118a-118f within the patient's mouth 100. The second intermediate components 120a-120f found within the provisional prosthesis 170 are placed over the first intermediate components 118a-118f still connected to the abutments 112a-112f connected to the plurality of implants within the patient's mouth 100. As the second intermediate components 120a-120f were removed from the first intermediate components 118a-118f after hardenable material was placed within the prosthetic template 160, alignment between the respective first intermediate components 118a-118f and the respective second intermediate components 120a-120f is precise.


The second intermediate components 120a-120f within the provisional prosthesis 170 may be secured to the first intermediate components 118a-118f via cement. Cement may be placed within ribs (e.g., 29a-29c FIG. 2) of the first intermediate components 118a-118f. The ribs allow the cement to fill the area between a bottom of the rib and a periphery of the first intermediate component. As the provisional prosthesis 170 is placed over the first intermediate components 118a-118f having cement within the ribs of the first intermediate components 118a-118f, the internal bore (e.g., 32FIG. 2) of the second intermediate components 120a-120f contacts the cement, further securing the second intermediate components 120a-120f within the provisional prosthesis 170 to the first intermediate components 118a-118f attached to the abutments 112a-112f.


Similarly, it is contemplated that cement may be placed within the internal bore 32 of the second intermediate components 120a-120f, and as the provisional prosthesis 170 is placed over the first intermediate components 118a-118f, the cement spreads into the ribs (e.g., 29a-29c FIG. 2) of each of the first intermediate components 118a-118f.


It is further contemplated that a press-fit or a snap-fit may be utilized to secure the second intermediate components within the provisional prosthesis to the first intermediate components attached to the abutments within the patient's mouth.


As shown in FIG. 8, the provisional prosthesis 170 has been secured within the patient's mouth 100. The provisional prosthesis 170 remains in the patient's mouth 100 until a final permanent prosthesis may be created in a laboratory setting. The provisional prosthesis 170 allows a patient to have a cosmetically pleasing functional prosthesis soon after surgery, thus improving a patient's recovery.


Once the final permanent prosthesis is prepared, the provisional prosthesis 170 and the first intermediate components 118a-118f are removed from the patient's mouth. The final prosthesis is typically adapted to be retained directly to the conical abutments 112a-112f via fastening screws that connect into the threaded portions 113a-113f of the conical abutments 112a-112f. Thus, the first intermediate components 118a-118f and the second intermediate components 120a-120f allow the conical abutment 112 to be used to support a provisional prosthesis, and upon completion of a permanent prosthesis, the conical abutment 112 may be used to directly support the permanent prosthesis.


While particular embodiments and applications of the present invention have been illustrated and described, it is to be understood that the invention is not limited to the precise construction and compositions disclosed herein and that various modifications, changes, and variations may be apparent from the foregoing descriptions without departing from the spirit and scope of the invention as defined in the appended claims.

Claims
  • 1. A method of creating a provisional dental prosthesis on an implant placed in bone comprising the acts of: retaining a conical abutment to the implant;securing a first intermediate component to the conical abutment;attaching a second intermediate component to the first intermediate component, the second intermediate component including a non-metallic material;placing a prosthetic template over the second intermediate component;filling the prosthetic template with a hardenable material;after the act of filling the prosthetic template, removing the prosthetic template with the second intermediate component within the hardenable material;forming a provisional prosthesis from the hardenable material, the provisional prosthesis containing the second intermediate component; andconnecting the provisional prosthesis to the first intermediate component by affixing the second intermediate component to the first intermediate component.
  • 2. The method of claim 1, wherein the first intermediate component comprises titanium.
  • 3. The method of claim 1, wherein the act of securing the first intermediate component uses a screw to secure the first intermediate component to the conical abutment.
  • 4. The method of claim 1, wherein the act of attaching the second intermediate component to the first intermediate component is a snap-fit.
  • 5. The method of claim 1, wherein the hardenable material is acrylic.
  • 6. The method of claim 1, wherein the prosthetic template has an inner cavity replicating a shape of teeth to be replaced by the prosthesis.
  • 7. The method of claim 1, wherein the act of removing the prosthetic template occurs after waiting a period of time for the hardenable material to at least partially solidify.
  • 8. The method of claim 1, wherein the act of connecting the provisional prosthesis to the first intermediate component includes placing cement between ribs of an outer periphery of the first intermediate component and the second intermediate component to secure the provisional prosthesis to the first intermediate component.
  • 9. The method of claim 1, wherein the second intermediate component is made entirely of a polymeric material.
  • 10. The method of claim 1 further comprising the acts of: removing the provisional prosthesis and the first intermediate component;attaching a permanent final prosthesis to the conical abutment.
  • 11. A method of forming a dental prosthesis on a plurality of implants placed in bone comprising the acts of: attaching a conical abutment to each of the plurality of implants;securing a metallic first intermediate component to each of the conical abutments;applying a second intermediate component to each of the metallic first intermediate components via a snap-fit;placing a provisional prosthetic template over the second intermediate components, the provisional prosthetic template forming an inner cavity generally replicating shapes of teeth replaced by the provisional prosthesis;filling the provisional prosthetic template with a hardenable acrylic material;removing the provisional prosthetic template with the second intermediate components from the mouth;forming a provisional prosthesis from the hardenable acrylic material, the provisional prosthesis containing the second intermediate components;connecting the provisional prosthesis to the metallic first intermediate components by placing the second intermediate components on the metallic first intermediate components;creating a permanent prosthesis;removing the provisional prosthesis and the metallic first intermediate components after the act of creating a permanent prosthesis; andattaching the permanent prosthesis to the conical abutments.
  • 12. The method of claim 11, wherein the metallic first intermediate component comprises titanium.
  • 13. The method of claim 11, wherein the act of connecting the provisional prosthesis to the metallic first intermediate component includes placing cement between the metallic first intermediate component and the second intermediate component to secure the provisional prosthesis to the first intermediate component.
  • 14. The method of claim 11, wherein at least one of the conical abutments is an angled abutment.
  • 15. The method of claim 11, wherein the metallic first intermediate components have a generally conical shape.
  • 16. The method of claim 15, wherein the metallic first intermediate components form a plurality of ribs about a periphery of the generally conical shape.
  • 17. The method of claim 11, wherein the second intermediate components are polymeric and have a generally conical shape.
  • 18. The method of claim 17, wherein the polymeric second intermediate components form a plurality of ribs about a periphery of the generally conical shape.
  • 19. The method of claim 11, wherein the metallic first intermediate components have a generally conical shape and form a plurality of ribs about a periphery of the generally conical shape, the second intermediate components have a generally conical shape and form a plurality of ribs about a periphery of the generally conical shape.
  • 20. The method of claim 19, wherein the act of connecting the provisional prosthesis to the metallic first intermediate component includes having cement within a gap between the plurality of ribs of the metallic first intermediate component and the second intermediate component to secure the provisional prosthesis to the first intermediate component.
  • 21. The method of claim 11, wherein the provisional prosthetic template forming an inner cavity generally replicating shapes of teeth replaced by the provisional prosthesis is formed from a stone model of a patient.
  • 22. The method of claim 11, wherein the provisional prosthetic template forming an inner cavity generally replicating shapes of teeth replaced by the provisional prosthesis is formed from a model of idealized teeth.
  • 23. A method of forming a provisional dental prosthesis on a plurality of implants placed in bone, the implants having abutments attached, the method comprising the acts of: securing a first intermediate component to each of the abutments;attaching a second intermediate component to each of the first intermediate components, the second intermediate component including a non-metallic structure;placing a provisional prosthetic template over the second intermediate components, the provisional prosthetic template forming an inner cavity generally replicating the shape of the provisional prosthesis;filling the provisional prosthetic template with a hardenable acrylic material to form a provisional prosthesis;removing the provisional prosthetic template.
  • 24. The method of claim 23, wherein the first intermediate component comprises titanium.
  • 25. The method of claim 23, wherein the act of securing the first intermediate component screws the first intermediate component to the abutment.
  • 26. The method of claim 23, wherein the act of attaching the second intermediate component to the first intermediate component is a snap-fit.
  • 27. The method of claim 23, wherein the act of attaching the second intermediate component to the first intermediate component is via cement.
  • 28. The method of claim 23, wherein the second intermediate component comprises PEEK.
  • 29. The method of claim 23, wherein the act of removing the provisional prosthetic template removes the second intermediate components from the first intermediate components allowing a practitioner to trim and polish the provisional prosthesis prior to use within the patient.
  • 30. The method of claim 23, wherein the act of attaching the second intermediate component to the first intermediate component is via cement and the second intermediate components remain attached to the first intermediate components following the act of removing the prosthetic template resulting in the provisional prosthesis being mounted to the first intermediate components via the second intermediate components.
US Referenced Citations (193)
Number Name Date Kind
3304608 Frohnecke Feb 1967 A
3958471 Willer May 1976 A
4011602 Rybicki et al. Mar 1977 A
4086701 Kawahara et al. May 1978 A
4177562 Miller et al. Dec 1979 A
4253833 Edelman Mar 1981 A
4306862 Knox Dec 1981 A
4341312 Scholer Jul 1982 A
4483675 Marshall Nov 1984 A
4547157 Driskell Oct 1985 A
4575340 Lustig Mar 1986 A
4624673 Meyer Nov 1986 A
4681542 Baum Jul 1987 A
4708654 Branemark Nov 1987 A
4713003 Symington et al. Dec 1987 A
4713004 Linkow et al. Dec 1987 A
4722688 Lonca Feb 1988 A
4738623 Driskell Apr 1988 A
4744753 Ross May 1988 A
D296362 Branemark Jun 1988 S
4758161 Niznick Jul 1988 A
4763788 Jorneus et al. Aug 1988 A
4767331 Hoe Aug 1988 A
4772204 Söderberg Sep 1988 A
4826434 Krueger May 1989 A
4842518 Linkow et al. Jun 1989 A
4850870 Lazzara et al. Jul 1989 A
4850873 Lazzara et al. Jul 1989 A
4856994 Lazzara et al. Aug 1989 A
4872839 Brajnovic Oct 1989 A
4955811 Lazzara et al. Sep 1990 A
4960381 Niznick Oct 1990 A
4988297 Lazzara et al. Jan 1991 A
4988298 Lazzara et al. Jan 1991 A
4995810 Soderberg Feb 1991 A
5000685 Brajnovic Mar 1991 A
5006069 Lazzara et al. Apr 1991 A
5015186 Detsch May 1991 A
5022860 Lazzara et al. Jun 1991 A
5026280 Durr et al. Jun 1991 A
5026285 Durr et al. Jun 1991 A
5030096 Hurson et al. Jul 1991 A
5035619 Daftary Jul 1991 A
5040983 Binon Aug 1991 A
5055047 Names Oct 1991 A
5061181 Niznick Oct 1991 A
5062800 Niznick Nov 1991 A
5071351 Green, Jr. et al. Dec 1991 A
5073111 Daftary Dec 1991 A
5100323 Friedman et al. Mar 1992 A
5104318 Piche et al. Apr 1992 A
5106300 Voitik Apr 1992 A
5116225 Riera May 1992 A
5122059 Dürr et al. Jun 1992 A
5125839 Ingber et al. Jun 1992 A
5125841 Carlsson et al. Jun 1992 A
5135395 Marlin Aug 1992 A
5145371 Jörnéus Sep 1992 A
5145372 Daftary et al. Sep 1992 A
5145612 Reay et al. Sep 1992 A
5154612 Carlsson et al. Oct 1992 A
5174755 Fukuda Dec 1992 A
5188800 Green, Jr. et al. Feb 1993 A
5195891 Sulc Mar 1993 A
5195892 Gersberg Mar 1993 A
5199873 Schulte et al. Apr 1993 A
5205745 Kamiya et al. Apr 1993 A
5209659 Friedman et al. May 1993 A
5209666 Balfour et al. May 1993 A
5213498 Pelerin May 1993 A
5213502 Daftary May 1993 A
5246370 Coatoam Sep 1993 A
5259759 Jorneus et al. Nov 1993 A
5281140 Niznick Jan 1994 A
5286195 Clostermann Feb 1994 A
5292252 Nickerson et al. Mar 1994 A
5297963 Dafatry Mar 1994 A
5302125 Kownacki et al. Apr 1994 A
5316476 Krauser May 1994 A
5316477 Calderon May 1994 A
5322443 Beaty Jun 1994 A
5328371 Hund et al. Jul 1994 A
5334024 Niznick Aug 1994 A
5336090 Wilson, Jr. et al. Aug 1994 A
5338196 Beaty et al. Aug 1994 A
5344457 Pilliar et al. Sep 1994 A
5350297 Cohen Sep 1994 A
5350302 Marlin Sep 1994 A
5362234 Salazar et al. Nov 1994 A
5362235 Daftary Nov 1994 A
5362237 Chalifoux Nov 1994 A
5368483 Sutter et al. Nov 1994 A
5376004 Mena Dec 1994 A
5399090 Padros-Fradera Mar 1995 A
5417570 Zuest et al. May 1995 A
5419702 Beaty et al. May 1995 A
5431567 Daftary Jul 1995 A
5433606 Niznick et al. Jul 1995 A
5437550 Beaty et al. Aug 1995 A
5437551 Chalifoux Aug 1995 A
5458488 Chalifoux Oct 1995 A
5476382 Daftary Dec 1995 A
5476383 Beaty et al. Dec 1995 A
5478237 Ishizawa Dec 1995 A
5489210 Hanosh Feb 1996 A
5492471 Singer Feb 1996 A
5503558 Clokie Apr 1996 A
5533898 Mena Jul 1996 A
5538426 Harding et al. Jul 1996 A
5547377 Daftary Aug 1996 A
5556280 Pelak Sep 1996 A
5564921 Marlin Oct 1996 A
5564923 Grassi et al. Oct 1996 A
5564924 Kwan Oct 1996 A
5573401 Davidson et al. Nov 1996 A
5588838 Hansson et al. Dec 1996 A
5636989 Somborac et al. Jun 1997 A
5639237 Fontenot Jun 1997 A
5642996 Mochida et al. Jul 1997 A
5651675 Singer Jul 1997 A
5662475 Mena Sep 1997 A
5662476 Ingber et al. Sep 1997 A
5674069 Osorio Oct 1997 A
5674071 Beaty et al. Oct 1997 A
5674073 Ingber et al. Oct 1997 A
5683249 Ibsen et al. Nov 1997 A
5685715 Beaty et al. Nov 1997 A
5688123 Meiers et al. Nov 1997 A
5695336 Lazzara et al. Dec 1997 A
5702346 Lazzara et al. Dec 1997 A
5709547 Lazzara et al. Jan 1998 A
5725375 Rogers Mar 1998 A
5727943 Beaty et al. Mar 1998 A
5733124 Kwan Mar 1998 A
5749732 Sendax May 1998 A
5752830 Suarez May 1998 A
5759034 Daftary Jun 1998 A
5762500 Lazarof Jun 1998 A
5779480 Groll et al. Jul 1998 A
5782637 Cosenza Jul 1998 A
5782918 Klardie et al. Jul 1998 A
5788494 Phimmasone Aug 1998 A
5816809 Sapkos Oct 1998 A
5823777 Misch et al. Oct 1998 A
5829977 Rogers et al. Nov 1998 A
5829981 Ziegler Nov 1998 A
5842864 Unger Dec 1998 A
5846079 Knode Dec 1998 A
5868572 Lazzara et al. Feb 1999 A
5873722 Lazzara et al. Feb 1999 A
5873727 Barlow Feb 1999 A
5879161 Lazzara Mar 1999 A
5899695 Lazzara et al. May 1999 A
5899697 Lazzara et al. May 1999 A
5904483 Wade May 1999 A
5906489 Khazzam et al. May 1999 A
5927979 Misch et al. Jul 1999 A
5934906 Phimmasone Aug 1999 A
5938443 Lazzara et al. Aug 1999 A
5944525 Ura Aug 1999 A
5947736 Behrend Sep 1999 A
5964591 Beaty et al. Oct 1999 A
6030219 Zuest et al. Feb 2000 A
6068478 Grande et al. May 2000 A
6068480 Misch et al. May 2000 A
6083004 Misch et al. Jul 2000 A
6120293 Lazzara et al. Sep 2000 A
6142782 Lazarof Nov 2000 A
6149433 Ziegler et al. Nov 2000 A
6155828 Lazzara et al. Dec 2000 A
6159010 Rogers et al. Dec 2000 A
6217331 Rogers et al. Apr 2001 B1
6227856 Beaty et al. May 2001 B1
6247932 Sutter Jun 2001 B1
6276938 Jorneus et al. Aug 2001 B1
6280195 Broberg et al. Aug 2001 B1
6299447 Zuest et al. Oct 2001 B1
6325628 Morgan Dec 2001 B1
6332777 Sutter Dec 2001 B1
6461160 Sutter Oct 2002 B1
6488501 Harding Dec 2002 B1
6655962 Kennard Dec 2003 B1
6663388 Schar et al. Dec 2003 B1
6726480 Sutter Apr 2004 B1
6974322 May et al. Dec 2005 B2
6981873 Choi et al. Jan 2006 B2
20020106610 Hurson Aug 2002 A1
20040137406 Kennard Jul 2004 A1
20050181334 Jacobs Aug 2005 A1
20050202370 Brajnovic Sep 2005 A1
20050266382 Soler et al. Dec 2005 A1
20060228672 Hurson Oct 2006 A1
20070190489 Riley et al. Aug 2007 A1
Foreign Referenced Citations (40)
Number Date Country
679117 Dec 1991 CH
12 32 314 Jan 1967 DE
15 41 2 25 Apr 1970 DE
2 114 323 Oct 1971 DE
31 106 93 Sep 1982 DE
31 10694 Sep 1982 DE
35 31 389 Mar 1987 DE
40 28 855 Mar 1992 DE
19 742 381 Feb 1999 DE
0 190 670 Aug 1986 EP
0 442 855 Aug 1991 EP
0 473 262 Mar 1992 EP
0 657 146 Jun 1995 EP
0 727 193 Aug 1996 EP
0 814 724 Jan 1998 EP
0 879 025 Nov 1998 EP
1 463 860 Jul 1965 FR
1 291 470 Oct 1972 GB
2 252 501 Aug 1992 GB
WO 8502337 Jun 1985 WO
WO 88 03007 May 1988 WO
WO 93 20774 Oct 1993 WO
WO 9619946 Jul 1996 WO
WO 9619947 Jul 1996 WO
WO 9629019 Sep 1996 WO
WO 9629020 Sep 1996 WO
WO 9701306 Jan 1997 WO
WO 9706930 Feb 1997 WO
WO 9714371 Apr 1997 WO
WO 9720518 Jun 1997 WO
WO 9727816 Aug 1997 WO
WO 9728755 Aug 1997 WO
WO 9728756 Aug 1997 WO
WO 9831296 Jul 1998 WO
WO 9832393 Jul 1998 WO
WO 9836701 Aug 1998 WO
WO 9852490 Nov 1998 WO
WO 9904723 Feb 1999 WO
WO 9929255 Jun 1999 WO
WO 0217814 Mar 2002 WO
Related Publications (1)
Number Date Country
20090047630 A1 Feb 2009 US