Abstract: This disclosure relates to a milling blank for the production of medical-technical molded parts, in particular dental splints or ear molds, as well as a method for the production of such a blank.

Abstract: The invention is related to a casting form (1) for the generation of an ear piece (100or a part of an ear piece (100), wherein the ear piece (100) comprises a contact section (120) and a non-contact section (110). The casting form (1) comprises an inner surface (10) delimiting an inner volume (12) for receiving a casting material, wherein the inner volume (12) is at least a part of the contact section (120). The inner surface (10) comprises at least one profiled section (20) comprising at least one texturing element (30). The invention is further related to a method for generating a casting form (1). The invention further comprises an ear piece (100).

Abstract: The invention relates to a method for partial curing of an initial photoreactive material for 3D printing, comprising the steps of: a) providing an item (1) comprising the initial photoreactive material for 3D printing, b) a partial irradiation step comprising irradiating at least one curing section (20) of the initial photoreactive material for 3D printing of the item with a curing irradiation, yielding at least one cured section (120) of a partially-cured item (10), and at least one semi-curing section (40) of the initial photoreactive material of the item is irradiated with a semi-curing irradiation, yielding at least one semi-cured section (140) of the partially-cured item.

Abstract: The invention relates to an adaptation system (500), comprising a mouthpiece (10), configured to be positioned in a mouth of a person, and an external sensoring device (20). The external sensoring device (20) is configured to be positioned at the person, wherein the external sensoring device (20) comprises at least one sensor (22) configured to sense at least one measurable quantity when the mouthpiece (10) is positioned in the person's mouth and the external sensoring device (20) is positioned at the person. Further, the adaptation system (500) comprises an analysis device (30) configured to determine a compliance of the adaptation system and/or to determine an orientation of an upper jaw (100) and a lower jaw (200) to each other derived from the at least one sensed measurable quantity.

Abstract: This disclosure relates to a milling blank for the production of medical-technical molded parts, in particular dental splints or ear molds, as well as a method for the production of such a blank.

Abstract: A milling blank for producing medical-technical molded parts made from a material produced from at least two components, wherein a first component A comprises a poly(alkyl methacrylate) polymer, and wherein a second component B comprises at least one alkyl acrylate monomere and/or one alkyl methacrylate monomer, in which the poly(alkyl methacrylate) polymer of component A is at least partially soluble, wherein the material comprises a flexibilizer as a further component, wherein the flexibilizer is selected from the group of citric-acid-based, adipic-acid-based, phthalic-acid-based or aliphatic esters.

Abstract: A milling blank for producing medical-technical molded parts made from a material produced from at least two components, wherein a first component A comprises a poly(alkyl methacrylate) polymer, and wherein a second component B comprises at least one alkyl acrylate monomere and/or one alkyl methacrylate monomer, in which the poly(alkyl methacrylate) polymer of component A is at least partially soluble, wherein the material comprises a flexibilizer as a further component, wherein the flexibilizer is selected from the group of citric-acid-based, adipic-acid-based, phthalic-acid-based or aliphatic esters.

Abstract: The invention relates to a device and to a method for the production of a three-dimensional object by the consecutive layered bonding of a material that can be bonded by means of electromagnetic radiation, wherein in the so-called vat an at least n-phase system, where n>2, is present, of which at least one phase comprises the building material and at least one other a phase that cannot be mixed with the building material.

Abstract: A dental modal for making a dental prosthesis has a base body formed with model teeth and model gingiva and with a cutout in an edentate area and with a hole in a floor of the cutout. A plate is releasably fittable complementarily in the cutout and is formed with a hole aligned with the hole of the cutout. A gingiva mask is fittable on the plate in the cutout and is in turn formed with a hole aligned with the holes of the plate and of the cutout. A model implant insert is releasably fittable in the holes of the mask, plate, and cutout and carries a model implant or an implant-screw mockup.

Abstract: A dental modal for making a dental prosthesis has a base body formed with model teeth and model gingiva and with a cutout in an edentate area and with a hole in a floor of the cutout. A plate is releasably fittable complementarily in the cutout and is formed with a hole aligned with the hole of the cutout. A gingiva mask is fittable on the plate in the cutout and is in turn formed with a hole aligned with the holes of the plate and of the cutout. A model implant insert is releasably fittable in the holes of the mask, plate, and cutout and carries a model implant or an implant-screw mockup.

Abstract: Method for the production of a denture comprising the following steps:—collection of the biometric data of a patient, namely, the toothed or untoothed mandible and maxilla, the sizing of the jaws, the spatial position thereof relative to the skull, the condyle inclination and the movement of the mandible, and the recording of the mandible movement;—implementation of the data in a virtual articulator which is made available in the main memory of the data processing equipment;—CAD construction of the individual articulator preformed parts and dental molded bodies based on the collected patient data;—production of the individual articulator molded bodies and dental molded bodies by means of a generative manufacturing process based on the recorded biometric data;—incorporation of the individual articulator preformed parts and/or dental molded bodies into a standardized articulator housing, or complete generative manufacture of the articulator with individualized molded bodies.

Abstract: The invention relates to a device and to a method for the production of a three-dimensional object by the consecutive layered bonding of a material that can be bonded by means of electromagnetic radiation, wherein in the so-called vat an at least n-phase system, where n>2, is present, of which at least one phase comprises the building material and at least one other a phase that cannot be mixed with the building material.

Abstract: The invention relates to a biocompatible, low-viscosity, radiation-curable formulation for producing medical products, in particular adaptive ear pieces, otoplastic parts, shells or ear parts, by means of PNP methods or stereolithographic methods. Said formulation comprises: a) 15-60 wt. % of a monomeric or oligomeric dimethacrylate based on bisphenol A or bisphenol F; b) 0-50 wt. % one or more monomeric or oligomeric urethane (meth)acrylates with a functionality n<4, a viscosity <30 Pa s and a molecular weight <3500; c) 2-25 wt. % of a monomeric, aliphatic or cycloaliphatic dimethacrylate with a viscosity <3 Pa s; d) 2-35 wt. % of an iminooxadiazone dion derivative, characterised by 3 methacrylate and/or acrylate functions; 0-15 wt. % one or more monofunctional methacrylates; f) 0.5-6 wt. % of a photo initiator or a combination of photo initiators, whose absorption lies in the wavelength range of the laser beam that is used or the irradiation source; g) 0-0.5 wt.

Abstract: A two-component addition-crosslinking silicone comprises (a) 0.1-70% by weight polyorganosiloxanes containing at least two unsaturated groups in the molecule; (b) 0.1-15% by weight polyorganohydrogensiloxanes containing at least two SiH groups in the molecule; (c) 0.01-2.0% by weight noble metal catalyst; and (d) 0.1-5% by weight of a non-toxic antimicrobial additive or a combination of at least two non-toxic antimicrobial additives.

Abstract: A biocompatible, low-viscosity, radiation-curable composition for producing antimicrobial earpieces contains: a) 20-75 wt. % of one or a plurality of monomeric/oligomeric urethane(meth)acrylates having an acrylate functionality of <4, viscosity <30 Pa s, and molecular weight <3500; b) 5-45 weight % of a monomeric or oligomeric dimethacrylate of bisphenol A or bisphenol F and or of a monomeric aliphatic or cycloaliphatic di(meth)acrylate having a viscosity <6 Pa s; c) 2.5-25 weight % of a cross-linking monomeric or oligomeric component containing 4 methacrylate and/or acrylate functionalities; d) 0-15 wt. % of one or a plurality of monofunctional (meth)acrylates; e) 0.01-5 wt. % of one or a combination of antimicrobially active glass fillers and silver particles; and f) 0.5-6 wt. % of one or a plurality of photoinitiators whose absorption is in the wavelength range of an ND:YVO4 laser beam used or of an actinic radiation source used to promote free radical formation.

Abstract: The invention relates to a biocompatible, low-viscosity, radiation-curable formulation for producing medical products, in particular adaptive ear pieces, otoplastic parts, shells or ear parts, by means of PNP methods or stereolithographic methods. Said formulation comprises: a) 15-60 wt. % of a monomeric or oligomeric dimethacrylate based on bisphenol A or bisphenol F; b) 0-50 wt. % one or more monomeric or oligomeric urethane (meth)acrylates with a functionality n<4, a viscosity <30 Pa s and a molecular weight <3500; c) 2-25 wt. % of a monomeric, aliphatic or cycloaliphatic dimethacrylate with a viscosity <3 Pa s; d) 2-35 wt. % of an iminooxadiazone dion derivative, characterised by 3 methacrylate and/or acrylate functions; 0-15 wt. % one or more monofunctional methacrylates; f) 0.5-6 wt. % of a photo initiator or a combination of photo initiators, whose absorption lies in the wavelength range of the laser beam that is used or the irradiation source; g) 0-0.5 wt.

Abstract: The invention relates to a biocompatible, low-viscous, radiation curable formulation, particularly for use in stereolithography, for use in medical technology, in particular, for producing earpieces, containing: a) 55-95% by weight of a monomeric or oligomeric dimethacrylate based on bisphenol A or bisphenol F; b) 0-20% by weight of a urethane methacrylate having a functionality of n<4 and a viscosity<15 Pa s; c) 2-15% by weight of a monomeric aliphatic or cycloaliphatic dimethacrylate having a viscosity<5 Pa s; d) 0-15% by weight of a monofunctional methacrylate having a viscosity<3 Pa s; e) 0.5-6% by weight of a photoinitiator or a combination of a number of photoinitiators whose absorption is located within the wavelength range of the laser beam used; f) 0.

Abstract: The invention suggests a biocompatible, low-viscosity, radiation-curable composition for producing antimicrobial medical products, in particular earpieces, by means of PNP or generative production methods, containing: a) 0-75 wt. % of one or a plurality of monomeric/oligomeric urethane(meth)acrylates having a functionality of n <4, viscosity <30 Pa s, and molecular weight <3500; b) 0-5 wt. % of a monomeric or oligomeric dimethacrylate based on bisphenol A or bisphenol F and or of a monomeric aliphatic or cycloaliphatic di(meth)acrylate having a viscosity <6 Pa s; c) 0-25 wt. % of an n-fold cross-linking monomeric or oligomeric component, characterized by n3 3 meth- and/or acrylate functions; d) 0-15 wt. % of one or a plurality of monofunctional (meth)acrylates; e) 0.01-5 wt. % of one or a combination of antimicrobial additives from the groups of antimicrobially active glass fillers or silver particles; f) 0.5-6 wt.

Abstract: A two-component addition-crosslinking silicone comprises (a) 0.1-70% by weight polyorganosiloxanes containing at least two unsaturated groups in the molecule; (b) 0.1-15% by weight polyorganohydrogensiloxanes containing at least two SiH groups in the molecule; (c) 0.01-2.0% by weight noble metal catalyst; and (d) 0.1-5% by weight of a non-toxic antimicrobial additive or a combination of at least two non-toxic antimicrobial additives.

Abstract: The invention relates to a biocompatible, low-viscous, radiation curab]e formulation, particularly for use in stereolithography, for use in medical technology, in particular, for producing earpieces, containing: a) 55-95 % by weight of a monomeric or oligomeric dimethacrylate based on bisphenol A or bisphenol F; b) 0-20 % by weight of a urethane methacrylate having a functionality of n<4 and a viscosity<15 Pa s; c) 2-15 % by weight of a monomeric aliphatic or cycloaliphatic dimethacrylate having a viscosity<5 Pa s; d) 0-15 % by weight of a monofunctional methacrylate having a viscosity<3 Pa s; e) 0.5-6 % by weight of a photoinitiator or a combination of a number of photoinitiators whose absorption is located within the wavelength range of the laser beam used; f) 0.