Absstract of: US20260097192A1
An electronic device according to an example may comprises: a cartridge accommodation part for accommodating a cartridge including emulsion therein; a crushing circuit including a crushing element capable of crushing at least a portion of the cartridge arranged in the cartridge accommodating part; a processor for generating a crushing signal; a transfer circuit for transferring the crushing signal to the crushing circuit; and a microneedle for discharging, to the outside of the electronic device, the emulsion exposed by the crush of at least a portion of the cartridge.
Absstract of: US20260096729A1
Systems, devices, and methods including a processor having addressable memory, where the processor is configured to: generate a series of recordings using a plurality of sensors via receiving a set of full measurements at a scheduled recording time; assign a priority to each of the recordings based on detection of abnormalities; determine a new recording schedule based on the generated series of recordings and detected abnormalities in the processed series of recordings; transmit the generated series of recordings and associated flag indicating whether an abnormality is present in the generated series of recordings; determine abnormal health patterns based on continuous monitoring capabilities; and provide an alert about the abnormal health patterns.
Absstract of: WO2026075575A1
The current invention relates to electroconductive bioinks, as well as their method of obtaining and their use in food production. The described electroconductive bioinks feature a high capability for cell support, as well as excellent printability and high organoleptic and nutritional properties. The present invention also relates to a method of obtaining a food product through bioprinting by 3D extrusion of the electroconductive bioinks and of the resulting food product. The invention represents as an alternative to food production by 3D extrusion bioprinting associated to cellular agriculture techniques.
Absstract of: WO2026074268A2
The invention relates to a device comprising an expandable hollow hydrogel tube encapsulated by an ingestible capsule to enable the targeted delivery of large molecules such as biologics to the gastrointestinal (GI) mucosa. Upon ingestion, the capsule is arranged to release the hydrogel tube in the GI tract, where the hydrogel tube expands from a first configuration to a second configuration upon hydration. In its expanded state, the hydrogel tube exerts an outward radial force on the lining of the GI tract. In some embodiments, the outward-facing surface of the hydrogel tube comprises microneedles. The invention further relates to a hydrogel resin comprising: gelatin or poloxamer 407; a neutralisation agent; acrylic acid or sodium acrylate; a crosslinker; a photoinitiator; and a photoabsorber. The hydrogel tube of the invention may be produced by bioprinting and photo-crosslinking said hydrogel resin.
Absstract of: US20260100274A1
A system for configuring medical devices in a healthcare facility. The system receives a selection to configure one or more medical devices and generates a first electronic document that includes editable inputs for modifying one or more settings on the one or more medical devices. The system exports the first electronic document and receives one or more edits for modifying the one or more settings of the one or more medical devices and a signature. The system generates a second electronic document based on the one or more edits and exports the second electronic document for modifying the one or more settings of the one or more medical devices.
Absstract of: US20260096783A1
0000 An apparatus and method for subject monitoring and diagnosing with non-invasive measures are disclosed. The apparatus includes a memory contains instructions configuring at least a processor to generate invasive measurement training data, train an invasive measurement machine-learning model using the invasive measurement training data, receive non-invasive measurement data, wherein the non-invasive measurement data includes electrocardiogram (ECG) data and echocardiogram (echo) data and the non-invasive measurement data includes information that is obtained through non-invasive measurements, fuse the ECG data and the echo data into a fused non-invasive measurement datum, generate at least an invasive measurement datum as a function of the fused non-invasive measurement datum using the trained invasive measurement machine-learning model, wherein the at least an invasive measurement datum includes information that can be obtained through invasive measurements and transmitting the at least an invasive measurement datum to a remote device.
Absstract of: US20260096731A1
0000 Systems and methods for biometric analysis are described. In some embodiments, a system may include a wearable device configured to be worn on a portion of an arm of a user while the user sleeps. The wearable device may include a plurality of electrodes disposed on an interior of the wearable device and configured to obtain biopotential signals from the user's arm. The system also may include a processor configured to analyze biopotential data derived from the biopotential signals to determine one or more characteristics relating to sleep of the user, and generate an output based on the one or more characteristics relating to the sleep of the user.
Absstract of: US20260098923A1
The disclosure relates to devices and methods for applying a magnetic field on a body of a patient. The time-varying magnetic field may applied to a brain of the patient. The disclosure provides a method of finding the position suitable for application of the magnetic field to the brain. The devices and methods of the disclosure may be suitable for reducing of food craving.
Absstract of: US20260096780A1
0000 In accordance with a method of detecting a pressure induced sensor artifact (PISA) in an analyte trace, a measured analyte trace having a plurality of data samples obtained over a period of time from an analyte sensor is received. A reconstructed analyte trace and an associated confidence window is generated from the measured analyte trace using a Bayesian denoising algorithm that includes a model that models the measured analyte trace as a sum of an unknown true analyte trace and a measurement error. The measured analyte trace is compared to the reconstructed analyte trace to identify data samples in the measured analyte trace that are located outside of the confidence window as being associated with a PISA.
Absstract of: US20260097234A1
Presented herein are systems and methods for generating data structures for data structures for events detected across data sources in network environments. A computing system may maintain, on a data repository, a profile for a subject at risk of or diagnosed with cancer.The profile may identify a plurality of event identifiers for a corresponding plurality of events associated with administration of radiotherapy to the subject. The computing system may apply a prompt based on a request and at least a portion of the profile to a generative machine learning (ML) model. The computing system may generate, based on applying the prompt to the generative ML model, a data structure comprising (i) a plurality of nodes corresponding to the respective plurality of event identifiers and (ii) a plurality of edges each defining a relationship between a corresponding pair of the plurality of nodes.
Absstract of: US20260096919A1
0000 Disclosed is a dental appliance for treating a patient having obstructive sleep apnea or hypopnea. Also included is a method of preparing the dental appliance.
Absstract of: CN119863574A
The invention relates to the technical field of three-dimensional reconstruction, and provides a three-dimensional reconstruction method and device, electronic equipment and a storage medium, and the method comprises the steps: obtaining a first image frame set of an oral cavity in a first state, and the oral cavity in the first state represents that at least one actual scanning rod is installed in the oral cavity; identifying a scanning rod area of each image frame in the first image frame set; and based on the feature information in the scanning rod region, splicing the plurality of image frames in the first image frame set, and reconstructing to obtain target three-dimensional data corresponding to an actual scanning rod in the oral cavity. According to the method, splicing is carried out based on the rigid structure, the influence of anatomical structures (such as gingiva, lip and tongue) in the image frame on the splicing precision can be reduced, and the overall precision of three-dimensional reconstruction can be improved.
Absstract of: US20260100260A1
0000 Aspects of electronic illuminator systems and methods are disclosed herein, including subsystems, methods of use, and computer-readable media thereof. In one aspect, a system includes a fiber detection assembly. The system further includes a cap color detection assembly. The system further includes a printed circuit board connected to the fiber detection assembly and the cap color detection assembly. The system is configured to illuminate a cable engaged with the system with an effect corresponding to the cable upon authenticating the cable.
Absstract of: AU2026202071A1
A system for estimating greenhouse gas emission in an environment housing an animal population, the system comprising: one or more monitoring devices configured to monitor parameters of members of the animal population; a data repository 1 comprising one or more records, each of the records (i) being associated with a respective member of the members, and (ii) including one or more parameters of the respective member as monitored by at least one of the monitoring devices over time; and a processing circuitry configured to: obtain at least a subset of the records, the subset being associated with a group of members of the animal population; determine one or more greenhouse gas emission affecting parameters based on the subset; estimate an amount of greenhouse gas emission in the environment utilizing the greenhouse gas emission affecting parameters; and perform an action utilizing the estimated CA amount of greenhouse gas emission in the environment. ar Health Score Affectivity/ Happiness Natural Living Score Score Fig. 1 Network Interface 220 Welfare KPIs Determination Module Data Repository 210 Processing Circuitry 230 Welfare Determination System 200 Fig. 2 ar e t w o r k n t e r f a c e e t e r m i n a t i o n o d u l e
Absstract of: US20260096771A1
0000 Multi-layer contact patches, as well as related apparatus, kits, systems, and methods, enable improved allergen testing and diagnosis. Multi-layer contact patches include a shield layer releasably coupled to an adhesive layer. The adhesive layer at least partially defines and is fixably coupled to an allergen complex layer. The allergen complex layer defines a plurality of allergen complex cavities. At least a subset of the allergen complex cavities include an allergen complex positioned therein, each allergen complex comprising an absorbent matrix and an allergen.
Absstract of: AU2024354926A1
In one or more embodiments, aspects of the present disclosure describe an apparatus for generating a three-dimensional (3D) model of cardiac anatomy via machine-learning, wherein the apparatus includes a computing device configured to receive a set of images of a cardiac anatomy pertaining to a subject, generate a three-dimensional (3D) data structure representing the cardiac anatomy as a function of the set of images, generate an initial 3D model of the cardiac anatomy, refine the generated initial 3D model of the cardiac anatomy as a function of the 3D data structure representing the cardiac anatomy and generate a subsequent 3D model of the cardiac anatomy as a function of the refinement.
Absstract of: AU2023466489A1
An infusion system includes an infusion device and an electronic device. The electronic device is configured to receive an automated programming request (APR) that includes a fluid type, a disposable type, and an infusion device identifier. The electronic device is also configured to determine, based on the APR, an alarm threshold for triggering an alarm of the infusion device or a flow rate for pumping a fluid of the fluid type. Additionally, the electronic device is configured to modify the APR to include the alarm threshold or the flow rate and then transmit the modified APR to the infusion device. The infusion device is configured to, after receiving the modified APR, set the alarm to trigger at the alarm threshold, pump the fluid at the flow rate, or confirm the alarm threshold or the flow rate via a user interface presented at a display associated with the infusion device.
Absstract of: AU2024346428A1
Embodiments of the invention relate to cabinets that can store medications and medical devices in public spaces and provide easy access to their contents in emergencies while also deterring theft, vandalism, and damage to the contents. These goals may be furthered in connection with, e.g., one or more electronic systems included in the cabinet. These electronic systems may, according to embodiments of the invention, provide functions related to, e.g., summoning help in emergencies, monitoring access to the cabinet, monitoring environmental conditions around and/or with the cabinet, removing and replacing medications that have reached expiry, and replacing medications that have been used or otherwise removed from the cabinet.
Absstract of: US20260096666A1
0000 A bed can include a mattress and a foot warming system. The mattress can include a mattress cover and a support structure that is positioned under and covered by the mattress cover. The foot warming system can include a heating unit an envelope, a power source, and an electrical connector electrically connecting the heating unit to the power source. The heating unit can be positioned inside the envelope between the envelope top and the envelope bottom. The heating unit and the envelope can be positioned at a foot of the bed under mattress cover between the support structure and the mattress cover.
Absstract of: US20260096869A1
0000 A method of designing a patient removable tooth positioning appliance may include receiving a digital representation of teeth of the patient in a selected arrangement and modeling the patient removable tooth positioning appliance having tooth receiving cavities shaped to receive and apply a resilient positioning force to the teeth of the patient based on the digital representation. The method may also include modeling a hook integral to the patient removable tooth positioning appliance and configured to interface with an elastic member so as to react a force from the elastic member into the appliance. The hook may be configured to be laterally offset from a portion of a tooth receiving cavity of the tooth receiving cavities. The method may also include outputting a three-dimensional representation of the patient removable tooth positioning appliance having the hook for fabrication by one or more fabrication machines.
Absstract of: AU2024327483A1
Methods and apparatus for predicting decoupling during a non-cardiac medical procedure are provided. The method includes receiving one or more patient characteristics associated with a patient scheduled for a non-cardiac medical procedure, providing the one or more patient characteristics as input to a machine learning model trained to output a decoupling prediction, processing, using at least one computer processor, the one or more patient characteristics using the machine learning model to output a decoupling prediction for the patient, wherein the decoupling prediction is associated with the non-cardiac medical procedure, and displaying, on a user interface, an indication of the decoupling prediction for the patient output from the machine learning model.
Absstract of: US20260096854A1
Disclosed are methods and systems to provided planning tools for surgery, particularly for THA. Images of musculoskeletal structure of a patient (e.g. associated with respective planes and in a same or different functional position) may be displayed together and via co-registration and spatial transformations, 3D implants or other objects may be rendered and overlaid in a same position correctly with respect to each image. Measures may be represented with respect to various planes associated with the respective image and/or with respect to an existing implant. A safe zone (graphical element) may be rendered and overlaid with respect to each displayed image to indicate a clinically accepted safe range of positions for the 3D implant. Different instances of implants having respective characteristics affecting range of motion may be available for use during a procedure. For a set of available implants minimal and maximal safe zones may be presented for planning assistance.
Absstract of: WO2026074549A1
This invention, titled "Medical Identification and Signal Tag System", addresses the growing challenge of maintaining accurate and timely patient monitoring in high-stress clinical environments such as emergency rooms and operating theaters. The technical problem targeted by this invention stems from the overwhelming workload, fragmented patient data systems, and delayed response times that often lead to medical errors and professional burnout among healthcare workers. To overcome these limitations, the invention integrates an Advanced Monitoring Analytics Module with a Wearable Medical Identification Tag. The system automatically analyzes patients' vital signs using artificial intelligence and machine learning algorithms capable of detecting critical physiological changes in real time. These algorithms dynamically interpret multi-parameter inputs such as heart rate, blood pressure, oxygen saturation, and body temperature and issue immediate alerts to the medical staff through a secure wireless connection. Technically, the invention employs a dual-component architecture. The monitoring unit, attached to the hospital's existing patient monitor, collects and processes biosignals using a high-speed microcontroller and a neural processing unit (NPU). The second component, the wearable tag, communicates via BLE protocol and provides visual, vibrational, and digital alerts through LED indicators and an integrated LCD interface. A secure encryption layer ensures data confidentiality
Absstract of: US20260096910A1
0000 A prosthetic assembly includes a socket and a liner. The socket includes a first interlocking feature and defines an inner volume. The liner includes a second interlocking feature. The first interlocking feature and the second interlocking feature are configured to engage each other when the liner is inserted into the inner volume of the socket. The liner is configured to receive a distal limb of a patient. At least one of the socket or the liner include inner voids extending within walls of the socket or the liner.
Nº publicación: WO2026076473A1 09/04/2026
Applicant:
PEARL DIGITAL INC [US]
Absstract of: WO2026076473A1
The disclosed bracket comprises a customized pad with an offset-defined envelope surface and a plurality of retentive features. These retentive features may include protrusions, depressions, or discrete discontinuous structures, while fracture features and removal features are incorporated to facilitate controlled debonding. Such structural designs enhance adhesive contact, improve bonding strength, and enable easier, safer bracket removal at the end of orthodontic treatment.