Abstract: The present disclosure describes articles, systems, and techniques including an additive manufactured orthodontic attachment including a body defining a retaining member configured to retain the article in a recess defined by a shell of a transfer tray; a coupling portion configured to engage a tool for insertion of the attachment into the recess of the transfer tray; and a bonding surface configured to bond the attachment to a portion of an outer surface of a tooth of a patient.

Abstract: The present disclosure relates generally to chemical indicators. In particular, the chemical indicators are useful for monitoring sterilization processes. The chemical indicator includes a fluid pathway and a chamber comprises a chemical-indicating composition.

Abstract: A negative pressure wound therapy (NPWT) device for a deep abdominal wound. The compressive component includes a body having a first compressive profile. The body includes a plurality of removable portions of the material. The plurality of removable portions are configured to be selectively removed to form a pattern of voids to transform the first compressive profile of the body into a second compressive profile of the body based on the pattern of voids. The pattern of voids includes at least one void.

Abstract: An example removable dental appliance includes an appliance body configured to at least partially surround a plurality of teeth of a dental arch of a patient. The appliance body includes a shell shaped to engage a tooth in an initial position and a gingival ridge extending from a mesial interproximal region along a gingival edge of the shell to a distal interproximal region. The gingival ridge is configured to engage a lingual or labial surface of the tooth below a height of contour of the tooth to enable the appliance body to apply a force vector at a contact point on the tooth to cause movement of the tooth toward a desired position of the tooth when the removable dental appliance is worn by the patient.

Abstract: Disclosed embodiments relate to devices and systems for providing both negative-pressure therapy and instillation, In some embodiments, both negative-pressure and instillation may be provided to a tissue site in a low-profile context that may also prevent siphoning of instillation fluid during negative pressure application. For example, a single bridge may include a negative-pressure pathway with supports and an instillation pathway, and the instillation pathway may be configured with respect to the negative-pressure pathway so that at least a portion of the instillation pathway collapses upon application of negative pressure to the negative-pressure pathway. Collapse of at least a portion of the instillation pathway may be sufficient to close the instillation pathway.

Abstract: Described herein are embodiments of a wound dressing layer. The wound dressing layer may include an open-cell foam. The foam may have a 50% compression force deflection of not more than about 4.8 kPa. The foam may also have a density of at least 24 kg/m3. The foam may exhibit a density increase of a factor of at least 12 at about ?75 mmHg.

Abstract: A method of building up a physical object by additive manufacturing which has the steps of building up the object and at least one support structure layer by layer along a build axis. The support structure supports the object relative to a build platform. During building up the object and the at least one support structure a connection is provided between the support structure and the object by a plurality of layers each of which being a common layer of the object and the support structure.

Abstract: A wound therapy system and method for clearing fluids from a conduit includes a wound dressing apparatus, a pneumatic pump, a valve, and a controller. The wound dressing apparatus is fluidly coupled to a wound, the pump, and the valve. The controller is configured to determine a volume of instillation fluid that has been delivered to the wound, to operate the pneumatic pump and the valve to apply a negative pressure to the wound dressing apparatus to purge a first portion of the instillation fluid, and to operate the pneumatic pump and the valve during a purge operation to deliver a volume of air through the wound dressing apparatus that is approximately equal to or greater than the volume of instillation fluid to purge a second portion of the instillation fluid from the wound dressing apparatus.

Abstract: The present disclosure provides a build platform for use in an additive manufacturing device that is builds up an object from layers of a light-hardenable resin, wherein the build platform comprises a build surface for building up the object thereon, and wherein the build surface comprises a ceramic material. The disclosure also provides a method of making a build surface comprises a ceramic surface. Further, the disclosure provides additive manufacturing devices that include build platforms comprising ceramic material. The disclosure also describes articles made using the methods and devices described.

Abstract: Illustrative embodiments of a dressing for treating a tissue site may include a fluid transport layer, an offloading layer, and a liquid deflector. The offloading layer may be in fluid communication with the fluid transport layer, and the offloading layer may include a force offloading region and a target region. The liquid deflector may be positioned between the fluid transport layer and the offloading layer. The liquid deflector may be configured to deflect a liquid from the tissue site into contact with the target region of the offloading layer. The target region may be configured to expand for offloading forces at the tissue site. Other dressings, systems, and methods are disclosed.

Abstract: A computer system performs live natural language processing (NLP) on data sources that are complex, remotely stored, and/or large, while satisfying restrictive time constraints. The computer system divides the NLP process into a batch NLP process and a live NLP process. The batch NLP process operates asynchronously over the relevant data set, which may be complex, remotely stored, and/or large, to summarize information into a summarized NLP data model. When the live NLP process is initiated, live NLP process receives as input the relevant information from the summarized NLP data model, possibly along with other data. The prior generation of the summarized NLP data model by the batch NLP process enables the live NLP process to perform NLP within time constraints that could not have been satisfied if the batch NLP process had not pre-processed the data set to produce the summarized NLP data model.

Abstract: The present disclosure is directed to self-contained biological indicators wherein a single type of indicator is capable of being used for various sterilization conditions, including sterilization with steam and/or ethylene oxide. In some embodiments, a single type of biological indicator is capable of being used for different steam sterilization conditions having varied temperatures and sterilization cycles.

Abstract: Aspects of the present disclosure relate to a warming system including a warming device. The warming device includes a clinical garment comprising a body portion adapted to cover a portion of a patient, an inner surface for facing the patient, and an outer surface for facing away from the patient. The body portion includes sleeves sized and positioned for receiving the patient's arms and a torso portion adapted to cover an anterior torso of a patient. A first pneumatic convective device can be disposed adjacent to the inner surface of the clinical garment. The pneumatic convective device can include an opening formed in the clinical garment for admitting a stream of pressurized, warmed air into the first pneumatic convective device. The warming system can also have a second pneumatic convective device in a fully-folded configuration or partially-folded configuration and disposed on a portion of the clinical garment.

Abstract: In some embodiments, a dressing assembly may include a dressing bolster, an interface seal, and a base layer. The dressing bolster may include a first side, a second side, and a periphery. The interface seal may be coupled at the periphery of the dressing bolster. The base layer may include a base layer flange configured to be coupled to the dressing and to extend beyond the periphery of the dressing bolster. The dressing assembly may be suitable for treating a tissue site with reduced pressure and for creating an apposition force between a first portion of the tissue site and a second portion of the tissue site. Other systems, apparatus, and methods are disclosed.

Abstract: A partially transparent dressing includes a fluid management core having a first side and a second, wound-facing side. The fluid management core includes an absorbent material and a plurality of optically transparent windows. The dressing includes a barrier layer coupled to the first side and a patient interface layer coupled to the second side. A fluid communication port is disposed in the second side. An opening is disposed in the patient interface layer. The opening is configured to receive fluid from a wound.

Abstract: This disclosure includes wound dressings (18) and systems (10) with therapeutic gas and negative pressure sources for incision management. The dressing, which are configured to be coupled to tissue to facilitate delivery of oxygen to the tissue, comprise a manifold configured to permit communication of oxygen to the tissue the manifold (46) defining: a plurality of gas passageways (50); and a plurality of openings (62), one or more of which comprises a length (66) and a width (70) that is at least 50 percent less than the length; and a gas-occlusive layer (86) configured to be disposed over the manifold and coupled to the tissue such that an interior volume containing the manifold is defined between the gas-occlusive layer and the tissue and the gas-occlusive layer limits escape of oxygen from the interior volume.

Abstract: The invention relates to a glazing composition suitable for glazing the surface a dental zirconia article. The glazing composition comprises a liquid, glass particles, and hydrophilic silica nano-particles. The invention also relates to a process for sintering a porous dental zirconia article with a glazing composition on its surface.

Abstract: A process of producing a surface-modified 3-dimensional article, the process comprising the steps of providing a radiation-curable composition, building-up a 3-dimensional article by radiation-curing the radiation-curable composition layer by layer, preferably by using a stereolithography or digital light processing unit, partially removing radiation-curable composition which sticks to the surface of the 3-dimensional article, treating only a portion of the surface of the 3-dimensional article to which the radiation-curable composition is stuck with particles, applying an additional curing step to the 3-dimensional article, preferably by applying heat and/or radiation. A 3-dimensional article which can be obtained by such a process and a kit of parts comprising such a 3-dimensional article.

Abstract: A process for producing a sintered lithium disilicate glass ceramic dental restoration by way of sintering under reduced atmospheric pressure conditions at a temperature above 600° C. is described. Further described is a kit of parts for producing a sintered lithium disilicate glass ceramic dental restoration.

Abstract: The disclosed tube securement device attaches to the patient's body and to the tube, while allowing for a section of the tube to be detached from the tube securement device. The tube securement device comprises a backing with adhesive coated sections. The backing comprises a first end section, a second end section, and a midsection, separating the first end section from the second end section. The tube securement device further comprises a first adhesive on at least a portion of the first major surface of the first end section, a second adhesive on at least a portion of the first major surface of the second end section, and wherein the first major surface of the midsection is free of tacky adhesive.