Systems, methods, and devices for improved orthodontic treatment of a patient's teeth are provided herein. In some embodiments, a method includes determining an appliance geometry for a dental appliance. The appliance geometry can include a first region representing a shell comprising a plurality of teeth receiving cavities, and a second region representing at least one integrally formed component to be integrally joined to the shell. The method can also include generating instructions including a first digital representation of the shell based on the first region, and a second digital representation of the at least one integrally formed component based on the second region. The method can further include transmitting the instructions to a fabrication system configured to additively manufacture the dental appliance by fabricating the shell based on the first digital representation, concurrently with fabricating the at least one integrally formed component based on the second digital representation.

An integrated testing device and fluid module are disclosed, as well as a method of manufacture. Fluid module contains a reservoir containing a test fluid, and a control vessel. The reservoir discharges test fluid into the control vessel, which discharges the test fluid in a controlled way to a test component.

A filming method of probe and the probe made by the filming method, the method includes following steps: spraying hydrophilic matrix material on the rigid member; injecting liquid polyethylene glycol into an interior, letting the polyethylene glycol coagulate; cutting out the solid polyethylene glycol, letting the cutting surface and the perimeter of the rigid member to be formed in a smooth plane; letting the wedge end of the rigid member insert a liquid latex vertically for immersion, picking up the rigid member and dripping residue, air drying the adhesive layer of the rigid member; upward setting the wedge end of the rigid member, and letting the latex film be heated, melting the solid polyethylene glycol and letting the polyethylene glycol drain away. The method can minimize the nonlinear deviation, simplify the technological process, improves product quality and manufacturing efficiency.

A system and method for forming a medical implant using a printing device. The printing device includes a print head having a heated nozzle, a heated build plate for receiving the printed material thereon, and a reflective plate having an active heater. A method for forming a medical device includes extruding a printing material by contiguous deposition to form a porous object having a lattice-like structure. The medical device, such as a spinal implant, may have interconnected pores and different regions, each having a different porosity for encouraging bone growth therein. The printed medical implant may be designed to be patient-specific, customized, and printed on-demand.

The present invention relates to a suspension comprising 50-95% by weight of the total suspension (w/w) of at least one metallic material and/or ceramic material and/or polymeric material and/or solid carbon containing material; and at least 5% by weight of the total suspension of one or more fatty acids or derivatives thereof. In addition, the invention relates to uses of such suspension in 3D printing processes.

The present invention belongs to the field of medical accessories, more precisely to the field of accessories for protection against outer conditions such as impacts, high or low temperature and similar conditions that can harm a human being. The invention relates to a personalized accessory for protection of a body part, which comprises a protective element, which fits to the shape of the excrescence, a scar or a wound, and an adjustable part to which the protective part is attached, glued, sewed or inserted, wherein the adjustable part can be stretched or in any other way adjusted to the particular body part, which has to be protected. The said accessory is manufactured in the following way: first the body part with the injury is scanned or measured in order to obtain a 3D model of the scanned or measured body part. Then the protective element is made using a 3D printer or thermoforming with an adjustable mould, wherein the finished protective element is then attached to the adjustable part.

The invention is for a synthetic composite for a bone graft comprising of: bio inert polymers comprising poly lactic acid, poly D, L-Lactic acid; bio active polymer consisting of polypropylene fumarate or diester of fumaric acid and propylene diol (1,2-Diol); and a bioactive inorganic component consisting of a metal fluorophosphates glass powder wherein the amount of the bioactive components is upto 30% (w/w) of the composite. The bioactive inorganic metal fluorophosphates glass powder of the composite is one of zinc fluorophosphate, magnesium fluorophosphate or silver fluorophosphate. The invention pertains to the method of making the scaffold, and also the 3D printed scaffold.

A system includes a partial enclosure configured to hold resin. The system further includes one or more structures configured to at least partially cover the resin. The one or more structures are configured to prevent evaporation of the resin. The system further includes a build platform configured to support an object that is being formed from layers of the resin. A first blade is configured to provide the layers of the resin to form the object on the build platform.

A method of production of a tissue sealing patch is disclosed. The method comprises applying a vacuum to a heated work surface; applying a solution of a biocompatible polyurethane polymer to the work surface and spreading it over the work surface with a polymer blade; evaporating the solvent; heating the work surface above the softening temperature of the polymer; spreading powdered tissue sealant material over the polymer film; incorporating the tissue sealant material to a depth of 20-60 μm in the film by pressing on a release sheet placed over the powder and polymer film; removing the release sheet from the adhesive patch material; releasing the vacuum; cooling said work surface; and removing the adhesive patch material from said work surface. The biocompatible polymer preferably comprises PEG-caprolactone-lactic acid units connected by urethane linkages, the PEG having a molecular weight of 3000-3500 amu, and a CL:LA:PEG ratio of 34:2:1.

The invention relates to a computer-implemented method for adjusting a position of artificial teeth of a denture. A digital 3D model of the denture comprising at least a denture part is provided. The denture part is configured for a jaw of a patient and comprises a dental arch with a plurality of artificial teeth arranged in an artificial gingiva. A deformable gingiva section of the artificial gingiva is defined between the teeth of the plurality of artificial teeth and a fixed gingiva section of the artificial gingiva with a fixed geometrical form. The dental arch is moved as a whole relative to the fixed gingiva section in order to adjust the position of the dental arch. A geometrical form of the deformable gingiva section is deformed due to the moving of the dental arch, whereas the fixed gingiva section maintains the fixed geometrical form.