JPH0549650A - Production of dental prosthetic appliance - Google Patents

Production of dental prosthetic appliance

Info

Publication number
JPH0549650A
JPH0549650A JP21497991A JP21497991A JPH0549650A JP H0549650 A JPH0549650 A JP H0549650A JP 21497991 A JP21497991 A JP 21497991A JP 21497991 A JP21497991 A JP 21497991A JP H0549650 A JPH0549650 A JP H0549650A
Authority
JP
Japan
Prior art keywords
porcelain
dental prosthesis
mixture
core material
molding
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
JP21497991A
Other languages
Japanese (ja)
Inventor
Koji Hakamazuka
康治 袴塚
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Olympus Corp
Original Assignee
Olympus Optical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Olympus Optical Co Ltd filed Critical Olympus Optical Co Ltd
Priority to JP21497991A priority Critical patent/JPH0549650A/en
Publication of JPH0549650A publication Critical patent/JPH0549650A/en
Withdrawn legal-status Critical Current

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  • Dental Prosthetics (AREA)

Abstract

PURPOSE:To provide the process for production of the dental prosthetic appli ance which can produce the dental prosthetic appliance having an excellent aesthetic property and high mechanical strength. CONSTITUTION:A core material 12 formed by casting and molding castable ceramics in accordance with the conventional method, then subjecting the molding to a crystallization treatment by heating the molding at 920 deg.C is disposed on an abutment tooth pattern 11. A porcelain mixture 13 prepd. by mixing porcelain 'Bitadule-N(R)' produced by Bita Co., porcelain 'Duceram(R)' correction powder (K) produced by Ducera Co., and low fusing graze material 'Ceracom Fine Grating Stain(R)' produced by Ceracom Co., at 7:2:1 weight ratio is then built up. After this mixture is cried for minutes at 600 deg.C, the mixture is heated up to 905 deg.C at 50 deg.C ratio per minute under a reduced pressure (760mmHg). The molding is then held for 30 minutes at 905 deg.C and is slowly cooled in the atm., by which the dental prosthetic appliance 10 is obtd.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、歯科用補綴物の製造方
法に関する。
FIELD OF THE INVENTION The present invention relates to a method for manufacturing a dental prosthesis.

【0002】[0002]

【従来の技術】従来、罹患した歯または脱落した歯を修
復するために用いられる歯科用補綴物は、例えば、次の
ようにして製造されている。まず、図2に示す如く、罹
患した歯を切削して作製した支台歯から採得した印象に
基づいて支台歯模型21を作製する。次に、支台歯模型
21の上に、支台歯を覆うような形状の金属製のコア材
22を作製する。次いで、コア材22の上に、コア材2
2の金属色を遮蔽するためのオペーク陶材23と、天然
歯の象牙質(デンチン)に対応する象牙質様陶材24、
天然歯のエナメル質に対応するエナメル質様陶材25お
よび透過性を引き出すための透明陶材(トランスルーセ
ント)26を順次築盛する。この後、陶材を焼き付けて
歯科用補綴物20を得ている。
2. Description of the Related Art Conventionally, a dental prosthesis used for repairing an affected tooth or a missing tooth is manufactured, for example, as follows. First, as shown in FIG. 2, an abutment tooth model 21 is produced based on an impression taken from an abutment tooth produced by cutting an affected tooth. Next, on the abutment tooth model 21, a metal core material 22 having a shape covering the abutment tooth is manufactured. Then, on the core material 22, the core material 2
Opaque porcelain 23 for shielding the metallic color of 2, and dentine-like porcelain 24 corresponding to the dentine of natural teeth,
An enamel-like porcelain material 25 corresponding to the enamel of natural teeth and a transparent porcelain material (translucent) 26 for drawing out transparency are successively built up. Then, the porcelain is baked to obtain the dental prosthesis 20.

【0003】また、上述の歯科用補綴物20の製造方法
において、金属製のコア材に代えて、ガラスセラミック
スを鋳造成型してなるキャスタブルセラミックスを用い
ることも行われている。
In the method of manufacturing the dental prosthesis 20 described above, castable ceramics formed by casting glass ceramics is also used in place of the metal core material.

【0004】[0004]

【発明が解決しようとする課題】上述の歯科用補綴物の
製造方法において、陶材を焼き付けると、隣接した陶材
粒子同士が結合して一体化される。しかし、結合した陶
材粒子の間には気孔が生じ易い。このため、完成した歯
科用補綴物の機械的強度および耐摩耗性が著しく低下す
る。
In the above-described method for manufacturing a dental prosthesis, when porcelain is baked, adjacent porcelain particles are bonded and integrated. However, porosity is likely to occur between the bonded porcelain particles. Therefore, the mechanical strength and wear resistance of the completed dental prosthesis are significantly reduced.

【0005】また、コア材としてキャスタブルセラミッ
クスを用いた場合、コア材の審美性を向上させるため
に、キャスタブルセラミックスの透明度を調整すること
が行われている。キャスタブルセラミックスの透明度
は、ガラス質のマトリックスと、結晶質の割合に応じて
変化するので、キャスタブルセラミックスを所定温度で
熱処理することにより、キャスタブルセラミックスの透
明度を調整することができる。しかし、キャスタブルセ
ラミックスの結晶化度が低いコア材の上に陶材を築盛し
た後、陶材の焼き付けを行うと、キャスタブルセラミッ
クスの結晶化がさらに進行する。このため、キャスタブ
ルセラミックスの色や透明度が変化したり、キャスタブ
ルセラミックスがさらに収縮する。この結果、歯科用補
綴物の色調を調整するのが困難であると共に、キャスタ
ブルセラミックスと陶材との界面に空隙が生じ、キャス
タブルセラミックスと陶材の適合性が悪化する等問題が
あった。
When castable ceramics are used as the core material, the transparency of the castable ceramics is adjusted in order to improve the aesthetics of the core material. Since the transparency of the castable ceramics varies depending on the glassy matrix and the ratio of the crystalline material, the transparency of the castable ceramics can be adjusted by heat-treating the castable ceramics at a predetermined temperature. However, when the porcelain is laid on the core material having low crystallinity of the castable ceramic and then the porcelain is baked, the crystallization of the castable ceramic further proceeds. For this reason, the color and transparency of the castable ceramics change, and the castable ceramics further contracts. As a result, there are problems that it is difficult to adjust the color tone of the dental prosthesis, and voids are generated at the interface between the castable ceramics and the porcelain, which deteriorates the compatibility between the castable ceramics and the porcelain.

【0006】本発明は、かかる点に鑑みてなされたもの
であり、より審美性に優れかつ機械的強度が高い歯科用
補綴物を製造することができる歯科用補綴物の製造方法
を提供するものである。
The present invention has been made in view of the above points, and provides a method for producing a dental prosthesis capable of producing a dental prosthesis which is more aesthetically pleasing and has high mechanical strength. Is.

【0007】[0007]

【課題を解決するための手段】本発明は、コア材の上
に、陶材およびグレーズ材の混合物を築盛した後、所定
温度で焼き付けることを特徴とする歯科用補綴物の製造
方法を提供する。ここで、グレーズ材としては、溶融温
度が800℃以下である低溶グレーズ材を用いるのが好
ましい。
SUMMARY OF THE INVENTION The present invention provides a method for manufacturing a dental prosthesis, characterized in that a mixture of porcelain and glaze material is built up on a core material and then baked at a predetermined temperature. .. Here, as the glaze material, it is preferable to use a low melting glaze material having a melting temperature of 800 ° C. or lower.

【0008】また、コア材としては、キャスタブルセラ
ミックスおよび金属を用いることができる。コア材がキ
ャスタブルセラミックスである場合には、キャスタブル
セラミックスを、陶材およびグレーズ材の混合物を焼き
付ける温度よりも高い温度で結晶化することが好まし
い。
Castable ceramics and metals can be used as the core material. When the core material is castable ceramics, it is preferable to crystallize the castable ceramics at a temperature higher than the temperature at which the mixture of porcelain and glaze material is baked.

【0009】[0009]

【作用】本発明の歯科用補綴物の製造方法によれば、陶
材にガラス質のグレーズ材が配合されているので、陶材
を焼き付けたときに結合した陶材粒子の間に生じた気孔
がグレーズ材によって埋められる。これにより、歯科用
補綴物の表面の機械的強度を向上できる。
According to the method for manufacturing a dental prosthesis of the present invention, since the vitreous glaze material is mixed with the porcelain, pores generated between the porcelain particles bonded when the porcelain is baked. Are filled with glaze material. Thereby, the mechanical strength of the surface of the dental prosthesis can be improved.

【0010】また、コア材としてキャスタブルセラミッ
クスを用いた場合には、キャスタブルセラミックスに、
陶材およびグレーズ材の混合物を焼き付ける温度よりも
高い温度で結晶化処理を施して、陶材およびグレーズ材
の混合物を焼き付ける温度ではそれ以上結晶化が進行し
なくなるまで、キャスタブルセラミックスを結晶化させ
る。これにより、陶材およびグレーズ材の混合物を焼き
付けるときに、キャスタブルセラミックスの結晶化度が
変化するのを防ぐことができる。
When castable ceramics is used as the core material, the castable ceramics are
The crystallization treatment is performed at a temperature higher than the temperature at which the mixture of porcelain and glaze is baked, and the castable ceramics are crystallized until the crystallization no longer progresses at the temperature at which the mixture of porcelain and glaze is baked. This can prevent the crystallinity of the castable ceramics from changing when baking the mixture of porcelain and glaze.

【0011】[0011]

【実施例】以下、本発明の実施例について、図面を参照
して詳細に説明する。図1は、本発明の歯科用補綴物の
製造方法に従って製造された歯科用補綴物の一例を示す
縦断面図である。
Embodiments of the present invention will now be described in detail with reference to the drawings. FIG. 1 is a longitudinal sectional view showing an example of a dental prosthesis manufactured according to the method for manufacturing a dental prosthesis of the present invention.

【0012】図1に示す如く、オリンパス光学株式会社
製のキャスタブルセラミックス(以下OCCと記す)H
−13(OCCの中で最も色が濃い材料)を常法に従っ
て鋳造した後、920℃で加熱して結晶化処理を施した
コア材12を、支台歯模型11の上に配置する。次い
で、コア材12の上に、ビタ社製の陶材ビタデュール−
N(商品名;VITADUR−N)、デュセラ(Duc
era)社製の陶材デュセラム(Duceram)修正
パウダー(K)およびセラムコ社製の低溶グレーズ材セ
ラムコ(商品名Ceramco)ファイングレインステ
イン(FINEGRAIN SATAIN)を、重量比
で7:2:1の割合で混合した陶材混合物13を築盛す
る。次に、600℃で5分間乾燥した後、減圧下(76
0mmHg)で毎分50℃の割合で905℃まで昇温し
た。次いで、905℃に30分間保持した後、大気中で
徐冷して、実施例1の歯科用補綴物10を得た。
As shown in FIG. 1, castable ceramics (hereinafter referred to as OCC) H manufactured by Olympus Optical Co., Ltd.
After casting -13 (the darkest material in OCC) according to a conventional method, the core material 12 which is heated at 920 ° C. and crystallized is arranged on the abutment model 11. Next, on the core material 12, Vita porcelain Vitadur made by Vita-
N (trade name; VITADUR-N), Ducera (Duc
era) porcelain Duceram modified powder (K) and low-melting glaze material Seramco (trade name Ceramco) fine grain stain (FINEGRAIN SATAIN) manufactured by Seramco in a ratio of 7: 2: 1 by weight. Build up the porcelain mixture 13 mixed in. Next, after drying at 600 ° C. for 5 minutes, it was dried under reduced pressure (76
The temperature was raised to 905 ° C at a rate of 50 ° C / min at 0 mmHg). Then, the temperature was maintained at 905 ° C. for 30 minutes and then gradually cooled in the atmosphere to obtain the dental prosthesis 10 of Example 1.

【0013】次に、OCCH−13を常法に従って鋳造
成型した後、920℃で加熱して結晶化処理を施したコ
ア材を、支台歯模型の上に配置する。次いで、コア材の
上にビタ社製の陶材ビタデュール−Nのみからなる陶材
を築盛する。次に、600℃で5分間乾燥した後、減圧
下(760mmHg)で毎分50℃の割合で960℃まで
昇温した。次いで、960℃に30分間保持した後、大
気中で徐冷して、比較例1の歯科用補綴物を得た。この
ようにして製造した実施例1および比較例1の歯科用補
綴物について、以下のような試験を行った。
Next, OCCH-13 is cast and molded according to a conventional method, and the core material which is heated at 920 ° C. and crystallized is placed on the abutment tooth model. Next, on the core material, a porcelain material made of Vita porcelain Vitadur-N alone is built up. Next, after drying at 600 ° C. for 5 minutes, the temperature was raised to 960 ° C. at a rate of 50 ° C./min under reduced pressure (760 mmHg). Then, after holding it at 960 ° C. for 30 minutes, it was gradually cooled in the atmosphere to obtain a dental prosthesis of Comparative Example 1. The following tests were performed on the dental prostheses of Example 1 and Comparative Example 1 manufactured in this way.

【0014】まず、実施例1および比較例1の歯科用補
綴物を、同じ条件で実体顕微鏡を用いて観察しところ、
実施例1の歯科用補綴物の陶材混合物13では、クラッ
クは認められなかった。これに対して比較例1の歯科用
補綴物では、大気中で徐冷した後にマージン部等の陶材
に微細なクラックが認められた。
First, the dental prostheses of Example 1 and Comparative Example 1 were observed under a stereoscopic microscope under the same conditions.
No cracks were observed in the porcelain mixture 13 of the dental prosthesis of Example 1. On the other hand, in the dental prosthesis of Comparative Example 1, fine cracks were observed in the porcelain material such as the margin after being gradually cooled in the atmosphere.

【0015】また、築盛部分を切削して切削面を実体顕
微鏡で観察したところ、実施例1の歯科用補綴物では、
結合した陶材粒子の間の気孔にグレーズ材が侵入して埋
め尽くされており、気孔は少なかった。しかし、比較例
1の歯科用補綴物では、多くの気孔が認められた。
Further, when the built-up portion was cut and the cut surface was observed with a stereoscopic microscope, the dental prosthesis of Example 1 showed that
The glaze material invaded and filled the pores between the bonded porcelain particles, and the pores were few. However, in the dental prosthesis of Comparative Example 1, many pores were recognized.

【0016】次に、実施例1および比較例1の歯科用補
綴物を、カーボランダムポイントを用いて研磨したとこ
ろ、実施例1の歯科用補綴物の陶材混合物13は粘りけ
があり、硬かった。これに対して、比較例1の歯科用補
綴物の陶材は、粘りけがなく、軟らかくぼろぼろと削れ
てしまった。
Next, when the dental prostheses of Example 1 and Comparative Example 1 were ground using carborundum points, the porcelain mixture 13 of the dental prosthesis of Example 1 was sticky and hard. .. On the other hand, the porcelain material of the dental prosthesis of Comparative Example 1 had no stickiness, was soft, and was shaved.

【0017】さらに、実施例1および比較例1の歯科用
補綴物について、ハブラシ摩耗試験のかわりに、耐摩耗
性の差を明確にするために、エンジンにアルミナホワイ
トペイントを取り付け、エンジンの回転数、回転時間を
一定にして、各歯科用補綴物の研削量を比較した。切削
は、テグサ社製歯科用マイクロモーターC2を用い、回
転数10000rpmで1分間行った後、切削表面を拡
大倍率16倍の実体顕微鏡で観察した。
Further, for the dental prostheses of Example 1 and Comparative Example 1, instead of the toothbrush abrasion test, alumina white paint was attached to the engine to clarify the difference in abrasion resistance. The grinding amount of each dental prosthesis was compared while keeping the rotation time constant. The cutting was performed using a dental micromotor C2 manufactured by Tegusa Co., Ltd. at a rotation speed of 10,000 rpm for 1 minute, and then the cutting surface was observed with a stereoscopic microscope with a magnification of 16 times.

【0018】この結果、実施例1の歯科用補綴物より
も、比較例1の歯科用補綴物の方が切削量が多いことが
確認され、実施例1の方が緻密な組織になっており、耐
摩耗性に優れていることが確認された。
As a result, it was confirmed that the dental prosthesis of Comparative Example 1 had a larger amount of cutting than the dental prosthesis of Example 1, and Example 1 had a denser structure. It was confirmed that the wear resistance was excellent.

【0019】このような試験結果から、陶材およびグレ
ーズ材を混合した陶材混合物を築盛した実施例1の歯科
用補綴物は、陶材だけを築盛した比較例1の歯科用補綴
物よりも、気孔が少なく、機械的強度および耐摩耗性に
優れていることが確認された。
From the above test results, the dental prosthesis of Example 1 in which the porcelain mixture in which the porcelain and the glaze material were mixed was built up more than the dental prosthesis of Comparative Example 1 in which only the porcelain was built up. It was confirmed that there were few pores and the mechanical strength and abrasion resistance were excellent.

【0020】次に、コア材12のOCCの結晶化温度
を、陶材混合物の焼き付け温度(905℃)よりも低い
880℃に設定して結晶化処理を施した以外は、実施例
1の歯科用補綴物と同じ材料を用い、同様の方法で製造
した比較例2の歯科用補綴物を試作し、陶材の色調を実
施例1の歯科用補綴物と比較した。この結果、実施例1
の歯科用補綴物では、当初予定した色調を得ることがで
きたが、比較例1の歯科用補綴物では、陶材混合物を焼
き付けたときに、コア材を構成するOCCの結晶化が進
行してコア材の色が微妙に変化し、予定した色調を得る
ことができなかった。この結果から、陶材混合物の焼き
付け温度よりも高い920℃で結晶化処理を施した実施
例1の歯科用補綴物のほうが色調の再現性に優れている
ことが確認された。
Next, except that the OCC crystallization temperature of the core material 12 was set to 880 ° C., which was lower than the baking temperature (905 ° C.) of the porcelain mixture, and the crystallization treatment was performed, the dentistry of Example 1 The dental prosthesis of Comparative Example 2 manufactured by the same method using the same material as the dental prosthesis was prototyped, and the color tone of the porcelain was compared with that of the dental prosthesis of Example 1. As a result, Example 1
In the dental prosthesis of No. 1, it was possible to obtain the initially planned color tone, but in the dental prosthesis of Comparative Example 1, when the porcelain mixture was baked, the crystallization of OCC constituting the core material proceeded. As a result, the color of the core material changed subtly, and the intended color tone could not be obtained. From this result, it was confirmed that the dental prosthesis of Example 1 which was subjected to the crystallization treatment at 920 ° C. higher than the baking temperature of the porcelain mixture was more excellent in color reproducibility.

【0021】また、実施例1の歯科用補綴物および比較
例2の歯科用補綴物において、コア材のOCCの結晶化
による収縮率を測定したところ、0CCを920℃で結
晶化した実施例1の歯科用補綴物では、約0.62%で
あり、0CCを880℃で結晶化した比較例2の歯科用
補綴物では約0.56%であった。この結果から、陶材
混合物の焼き付け温度よりも高い920℃で結晶化処理
を施した実施例1の歯科用補綴物のほうが、結晶化によ
る収縮率が大きく、陶材混合物を焼き付けるときには既
に収縮しているのでさらに収縮し難い。この結果、実施
例の歯科用補綴物は、完成時のコア材と陶材混合物の間
の適合性に優れていることが確認された。
Further, in the dental prosthesis of Example 1 and the dental prosthesis of Comparative Example 2, the shrinkage rate due to the crystallization of OCC of the core material was measured, and it was found that 0CC was crystallized at 920 ° C. The dental prosthesis of No. 2 was about 0.62%, and the dental prosthesis of Comparative Example 2 in which 0CC was crystallized at 880 ° C. was about 0.56%. From this result, the dental prosthesis of Example 1 that was subjected to the crystallization treatment at 920 ° C., which is higher than the baking temperature of the porcelain mixture, had a larger shrinkage rate due to crystallization, and already contracted when the porcelain mixture was baked. It is difficult to shrink further. As a result, it was confirmed that the dental prosthesis of the example had excellent compatibility between the core material and the porcelain mixture at the time of completion.

【0022】なお、本実施例では、便宜上、コア材12
の上に築盛された陶材混合物13を一体に形成した歯科
用補綴物について説明したが、本発明はこれに限定され
るものではなく、象牙質用陶材、エナメル質用陶材など
を順次積層した歯科用補綴物の製造にも適用することが
できる。
In this embodiment, for convenience, the core material 12 is used.
Although the dental prosthesis integrally formed with the porcelain mixture 13 laid on the above has been described, the present invention is not limited to this, and dentin porcelain, enamel porcelain and the like are sequentially formed. It can also be applied to the production of laminated dental prostheses.

【0023】[0023]

【発明の効果】以上説明した如くに、本発明の歯科用補
綴物の製造方法によれば、陶材にグレーズ材を配合する
ことにより、焼き付けにより結合した陶材粒子同士の間
に生じた気孔を、グレーズ材により埋めることができ
る。これにより、歯科用補綴物の機械的強度および耐摩
耗性を向上することができる。また、コア材にキャスタ
ブルセラミックスを使用した場合に、陶材およびグレー
ズ材の混合物を焼き付ける温度よりも高い温度で結晶化
処理を施すことにより、陶材およびグレーズ材の混合物
を焼き付ける際に、結晶化がさらに進行するのを防止し
て、歯科用補綴物の審美性をより向上させると共に、コ
ア材と築盛した陶材およびグレーズ材の混合物との適合
性を向上できる等顕著な効果を奏するものである。
As described above, according to the method for producing a dental prosthesis of the present invention, by mixing the porcelain with the glaze material, the pores generated between the porcelain particles bonded by baking are formed. Can be filled with a glaze material. Thereby, the mechanical strength and wear resistance of the dental prosthesis can be improved. In addition, when castable ceramics are used for the core material, crystallization is performed when baking the mixture of porcelain and glaze by performing crystallization treatment at a temperature higher than the temperature at which the mixture of porcelain and glaze is baked. Of the dental prosthesis and the compatibility of the core material with the built-up porcelain and glaze material can be improved. is there.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明の歯科用補綴物の製造方法に従って製造
された歯科用補綴物の一例を示す縦断面図。
FIG. 1 is a vertical cross-sectional view showing an example of a dental prosthesis manufactured according to the method for manufacturing a dental prosthesis of the present invention.

【図2】従来の歯科用補綴物の製造方法に従って製造さ
れた歯科用補綴物の一例を示す縦断面図。
FIG. 2 is a longitudinal sectional view showing an example of a dental prosthesis manufactured according to a conventional method for manufacturing a dental prosthesis.

【符号の説明】[Explanation of symbols]

10…歯科用補綴物、11…支台歯模型、12…コア
材、13…陶材混合物。
10 ... Dental prosthesis, 11 ... Abutment tooth model, 12 ... Core material, 13 ... Porcelain mixture.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 コア材の上に、陶材およびグレーズ材の
混合物を築盛した後、所定温度で焼き付けることを特徴
とする歯科用補綴物の製造方法。
1. A method for producing a dental prosthesis, which comprises laying a mixture of a porcelain material and a glaze material on a core material and then baking the mixture at a predetermined temperature.
【請求項2】 コア材がキャスタブルセラミックスであ
ることを特徴とする請求項1記載の歯科用補綴物の製造
方法。
2. The method for manufacturing a dental prosthesis according to claim 1, wherein the core material is castable ceramics.
【請求項3】 コア材を構成するキャスタブルセラミッ
クスに、陶材およびグレーズ材の混合物を焼き付ける温
度よりも高い温度で結晶化処理を施すことを特徴とする
請求項2記載の歯科用補綴物の製造方法。
3. The production of a dental prosthesis according to claim 2, wherein the castable ceramic constituting the core material is subjected to a crystallization treatment at a temperature higher than a temperature at which the mixture of the porcelain and the glaze material is baked. Method.
【請求項4】 コア材が金属であることを特徴とする請
求項1記載の歯科用補綴物の製造方法。
4. The method for manufacturing a dental prosthesis according to claim 1, wherein the core material is a metal.
JP21497991A 1991-08-27 1991-08-27 Production of dental prosthetic appliance Withdrawn JPH0549650A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21497991A JPH0549650A (en) 1991-08-27 1991-08-27 Production of dental prosthetic appliance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21497991A JPH0549650A (en) 1991-08-27 1991-08-27 Production of dental prosthetic appliance

Publications (1)

Publication Number Publication Date
JPH0549650A true JPH0549650A (en) 1993-03-02

Family

ID=16664713

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21497991A Withdrawn JPH0549650A (en) 1991-08-27 1991-08-27 Production of dental prosthetic appliance

Country Status (1)

Country Link
JP (1) JPH0549650A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09103438A (en) * 1995-09-15 1997-04-22 Dentsply Internatl Inc Artificial tooth, and die to form artificial tooth
JP2001233664A (en) * 2000-02-22 2001-08-28 Advance Co Ltd Ceramic having dense texture
JP2008206538A (en) * 2007-02-23 2008-09-11 Shiyoufuu:Kk Tooth with resin filling clearance between dentin layer and enamel layer
CN105997282A (en) * 2016-05-05 2016-10-12 张志帆 Processing method of porcelain tooth veneer
JP2020081895A (en) * 2018-11-29 2020-06-04 イフォクレール ヴィヴァデント アクチェンゲゼルシャフトIvoclar Vivadent AG Process for production of dental restoration

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09103438A (en) * 1995-09-15 1997-04-22 Dentsply Internatl Inc Artificial tooth, and die to form artificial tooth
JP2001233664A (en) * 2000-02-22 2001-08-28 Advance Co Ltd Ceramic having dense texture
JP2008206538A (en) * 2007-02-23 2008-09-11 Shiyoufuu:Kk Tooth with resin filling clearance between dentin layer and enamel layer
CN105997282A (en) * 2016-05-05 2016-10-12 张志帆 Processing method of porcelain tooth veneer
JP2020081895A (en) * 2018-11-29 2020-06-04 イフォクレール ヴィヴァデント アクチェンゲゼルシャフトIvoclar Vivadent AG Process for production of dental restoration

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