The disclosure relates to dental implantation, and more particularly to an adaptive element for dental implantation.
In conventional dental implantation, a first stage is to bury an implant, which is a metal post serving as a tooth root, in a patient's jaw bone by surgery.
After 3 to 6 months of osseointegration, the implant may become permanently stable, meaning that new bone has grown to the surface of the implant. Then, an abutment is attached to the implant for securing a dental crown (or prosthetic tooth). Lastly, the dental crown is connected to the abutment with lag screws or with dental cement.
In general, conventional abutments are designed to have standardized sizes and shapes. A dentist can only select one that matches the buried implant and most suitably fits the patient's gum. However, the fit may not be perfect so the selected conventional abutment may be too tight or too loose for the gum.
Therefore, an object of the disclosure is to provide a method for producing an adaptive element for dental implantation that can alleviate at least one of the drawbacks of the prior art.
According to the disclosure, the method includes steps of:
Other features and advantages of the disclosure will become apparent in the following detailed description of the embodiment(s) with reference to the accompanying drawings, of which:
Before the disclosure is described in greater detail, it should be noted that where considered appropriate, reference numerals or terminal portions of reference numerals have been repeated among the figures to indicate corresponding or analogous elements, which may optionally have similar characteristics.
Referring to
In step S1 of the method, the model creating equipment 11 creates a 3D virtual model 3 (see
In other embodiments, the model creating equipment 11 may be an intraoral scanner (not shown) which captures digital impressions and directly creates the 3D virtual model 3 according to the digital impressions thus captured. In further other embodiments, the model creating equipment 11 may be a conventional 3D scanner (not shown) that is used to create the 3D virtual model 3 based on a physical tooth model, which is obtained by conventional impression techniques.
Further referring to
The 3D virtual model 3 includes a crown part 31 and a root part 32 connected to the crown part 31. Specifically, the crown part 31 and the root part 32 of the 3D virtual model 3 correspond to a crown and a root of the to-be-treated tooth 51 or the missing tooth, respectively.
It should be noted that, in the case that the symmetric tooth 52 is designated as the target tooth, the image processor 112 initially creates an initial 3D model that corresponds to and represents the symmetric tooth 52 based on the images of the target tooth, and then creates a mirrored copy of the initial 3D model to serve as the 3D virtual model 3 that corresponds to the to-be-treated tooth 51 or the missing tooth.
In step S2, the processing device 12 obtains a boundary curve 33 between the crown part 31 and the root part 32 on the 3D virtual model 3. The boundary curve 33 corresponds to a boundary 522 (see
In one embodiment, the processing device 12 analyzes variation of the curvature of a facial surface of the 3D virtual model 3 to obtain the boundary curve 33 according to the variation of the curvature. It should be noted that the facial surface means the labial side for an anterior tooth (e.g., incisors and canines), and means the buccal side of a posterior tooth (e.g., molars and premolars). In some embodiments, an operator may manually mark a plurality of points between the crown part 31 and the root part 32 on the 3D virtual model 3, and the processing device 12 then connects the marked points to obtain the boundary curve 33 or constructs the boundary curve 33 that has the best fit to the marked points.
In step S3, the processing device 12 defines a boundary plane 35 on the root part 32 of the 3D virtual model 3 in a manner that the boundary plane 35 is spaced apart from the boundary curve 33 and is perpendicular to a vertical axis of the 3D virtual model 3. The vertical axis is defined in the coronal and apical directions of the tooth represented by the 3D virtual model 3. In one embodiment, the processing device 12 defines, as the boundary plane 35, a plane that is parallel to and spaced apart by a predetermined distance (h) from a tangent plane 34 touching a reference point 341 of the boundary curve 33 and perpendicular to the vertical axis, wherein the reference point 341 is an extremity of the boundary curve 33 on the facial surface of the 3D virtual model 3 in a direction parallel to the vertical axis. The predetermined distance (h) may be 3 mm, and may be adjusted on demand.
In step S4, the processing device 12 projects the boundary curve 33 on the boundary plane 35 in the direction parallel to the vertical axis. A virtual surrounding surface extending from the boundary curve 33 to the boundary plane 35 is defined as a projection periphery 351.
In step S5, the processing device 12 generates a tubular model 36 (see
The surrounding wall of the tubular model 36 has a predetermined thickness (t). In general, the predetermined thickness (t) may be preset to be 0.8˜1 mm, but not limited thereto.
In step S6, the 3D forming equipment 13, which may be a 3D printer, a turning process machine, or a molding machine, produces the adaptive element 37 (see
Referring to
After the resin 73 rigidifies, the dentist dismounts the integrated body 70. The integrated body 70 may be processed to remove a stage between the adaptive element 37 and the resin 73. Accordingly, the integrated body 70 that has been processed would have a smooth outer surface corresponding to the adaptive element 37 and a part of the resin 73 (see
Lastly, as shown in
As described above, in the embodiments of the present invention, a 3D virtual model 6 is constructed based on 3D images of a to-be-treated tooth 51 or a symmetric tooth 52 of the patient, a tubular model 67 is obtained from the 3D virtual model 6, and an adaptive element 37 for dental implantation is then produced according to the tubular model 67. Thus, the adaptive element 37 may be applied during dental implantation and the dental abutment 74 may be produced accordingly. Since the part of the dental abutment 74 which is mounted to the gums is produced according to the adaptive element 37, it may fit the hole in the gum part 511 of the patient very well. Further, since the stage between the adaptive element 37 and the resin 73 of the integrated body 70 has been removed (see
In the description above, for the purposes of explanation, numerous specific details have been set forth in order to provide a thorough understanding of the embodiment(s). It will be apparent, however, to one skilled in the art, that one or more other embodiments may be practiced without some of these specific details. It should also be appreciated that reference throughout this specification to “one embodiment,” “an embodiment,” an embodiment with an indication of an ordinal number and so forth means that a particular feature, structure, or characteristic may be included in the practice of the disclosure. It should be further appreciated that in the description, various features are sometimes grouped together in a single embodiment, figure, or description thereof for the purpose of streamlining the disclosure and aiding in the understanding of various inventive aspects, and that one or more features or specific details from one embodiment may be practiced together with one or more features or specific details from another embodiment, where appropriate, in the practice of the disclosure.
While the disclosure has been described in connection with what is (are) considered the exemplary embodiment(s), it is understood that this disclosure is not limited to the disclosed embodiment(s) but is intended to cover various arrangements included within the spirit and scope of the broadest interpretation so as to encompass all such modifications and equivalent arrangements.
Number | Date | Country | Kind |
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108122116 | Jun 2019 | TW | national |
109134171 | Sep 2020 | TW | national |
This application is a continuation-in-part of U.S. patent application Ser. No. 16/716,105, filed on Dec. 16, 2019, which claims priority of Taiwanese Invention Patent Application No. 108122116 filed on Jun. 25, 2019. This application further claims priority of Taiwanese Invention Patent Application No. 109134171, filed on Sep. 30, 2020.
Number | Name | Date | Kind |
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20150025855 | Fisker | Jan 2015 | A1 |
Number | Date | Country |
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1469833 | Dec 2014 | KR |
I686182 | Mar 2020 | TW |
WO2013112233 | Sep 2014 | WO |
Entry |
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Exocad (“exocad Video Tutorial (basic): Custom Abutment Design”, 2017) (Year: 2017). |
Mangano et al (“A novel full-digital protocol (SCAN-PLAN-MAKE-DONE®) for the design and fabrication of implant-supported monolithic translucent zirconia crowns cemented on customized hybrid abutments.” International Journal of Environmental Research and Public Health 16.3 (2019): 317 (Year: 2019). |
Organical (“Exocad 3D Printing Files”, Jun. 4, 2019) (Year: 2019). |
ExocadBrochure (“The complete software solution for digital dentistry”, 2015) (Year: 2015). |
Search Report appended to an Office Action, which was issued to Taiwanese counterpart application No. 109134171 by the TIPO dated Jun. 8, 2021, with an English translation thereof (2 pages). |
Number | Date | Country | |
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20210267726 A1 | Sep 2021 | US |
Number | Date | Country | |
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Parent | 16716105 | Dec 2019 | US |
Child | 17322638 | US |