Embodiments of the present disclosure are directed to devices, systems and methods for providing safety functionality in an exoskeleton system. In particular, some embodiments make use of a sensor system and methodology with/for an exoskeleton apparatus to facilitate such safety functionality. For example, a system for regulating a load amount applied on a user of an exoskeleton may comprise one or more sensors for sensing data related to an amount of force exerted at a limb of the user by a part of the exoskeleton; a communications component for transmitting the sensed data to a processing unit operably coupled to the exoskeleton; and the processing unit configured to process the data so as to determine the amount of exerted force and generate an instruction to trigger a mode of operation of the exoskeleton based on the determined amount of force.

Proposed is a vibration unit available for eyesight recovery glasses, the vibration unit being mounted on any one side or each of left and right eye sides of a frame unit of the eyesight recovery glasses, wherein the vibration unit is configured to generate ultrasonic waves through vibration. Accordingly, ultrasonic waves in a low frequency band are directly transmitted to the eyeball rather than inducing an eye movement, thereby being capable of providing the vibration unit available for the eyesight recovery glasses realizing a substantial eyesight recovery effect. In addition, the ultrasonic waves transmitted to the eyeball may help to relieve eye strain, to increase blood flow, and to activate eye cells.

A training device for carrying out a muscle training for a person's muscle. The training device includes a control unit having a signal unit, a main body, and a load measuring device arranged on the main body. The person's muscle contacts the load measuring device in use. The load measuring device has a load sensor which determines a load exerted by the person on the load measuring device at a measuring point which is correlated with a partial region of the muscle at a measuring point position. The control unit outputs a contraction signal to the person via the signal unit so that the person performs a signaled muscle contraction based thereon. A successful performance of the signaled muscle contraction is verifiable by comparing a load profile, which is determined by the load measuring device, with a comparison load profile.

A controller for a sexual stimulation device is disclosed. The controller includes: an input device formed as an artificial anatomical part, the input device including a plurality of touch sensors disposed thereon, the plurality of touch sensors being configured to generate output signals responsive to touch inputs on an external surface of the input device; and an attachment member for removably coupling the input device to a mobile electronic device, the mobile electronic device having a display on a first side, wherein the attachment member supports the input device over the first side of the mobile electronic device when the input device is secured to the mobile electronic device via the attachment member.

Disclosed a system (100) for enacting a positive and a negative pressure on a limb. The system (100) includes an air compressor (102) coupled to a reservoir (104), a piston assembly (106) configured to the reservoir (104), wherein the piston assembly (106) further comprises a piston (108) circumfused inside a tube (107), a pneumatic ring (114) coupled to the system (100) via the piston assembly (106) maintains intermittent pressure and prevents formation of a venous blood clot ischemic injury to a tissue distal to the pneumatic ring (114) compression due to lack of blood flow.

A method of treatment for congestive colon failure (CCF) including evaluating an origin of a lipase and/or an amylase from a biological fluid sample from the subject, optionally analyzing a level of the lipase and/or an amylase from the biological fluid sample from the subject, optionally imaging a colon and a pancreas of the subject and providing laxatives, an anti-fungal composition, fat, a composition selected from a group comprising glucosamine, methylsulfonylmethane (MSM) rhamnan sulfate, Sulodexide, Rosuvastatin, Metformin, Hydrocortisone, Antithrombin, Etanercept, Heparin, Albumin, Fresh frozen plasma (FFP), Poloxamer-188, vitamins, trace elements, a locally acting vasodilator, anaerobic microbial culture, pickled fruits, pickled vegetables, preserved meat, and fermented juices or a combination thereof based upon results of the first three steps.

Orthosis systems are disclosed, having a wearable assembly and a user replaceable orthosis effector assembly. The wearable assembly includes a motor mechanism and a coupler that is movable by the motor mechanism between a starting location and an unloading location. The coupler has a receiving space. The effector assembly couples to the wearable assembly and has a tension element that actuates the effector assembly. A first end of the tension element is seated in the receiving space of the coupler when the effector assembly is coupled to the wearable assembly. The first end of the tension element is releasable from the receiving space when the coupler is in the unloading location, decoupling the effector assembly from the wearable assembly.

A human sleep monitoring device, including a signal processing module (5), a reflecting film (3), a detection light emitting module (1) and a receiving module (4), wherein the detection light emitting module (1) is configured to emit detection light to the human body; the reflecting film (3) is configured to guide light, which is emitted by the detection light emitting module and not absorbed by the human body, to the receiving module (4); the receiving module (4) is configured to receive the light guided by the reflecting film (3); and the signal processing module (5) is configured to obtain physiological sign data of the human body according to intensity information of the light received by the receiving module (4). The device can monitor the sleep state of the human body in real time, and improve body sleep quality. A human sleep monitoring method is also provided.

The present disclosure relates to an organism trapping device that includes a vibration wave generator configured to generate frequency ranges from 1.00 to 1.67 Hz (Hertz), an inciting engine communicatively coupled with the vibration wave generator, and configured to generate signals representing vibration parameters based on the generated frequency, a walled container operatively coupled with the inciting engine and adapted to contain fluid and receives the generated signals to simulate flow of blood in human blood vessels based on the vibration parameters to attract number of organisms towards the device, a fumigating agent adapted to compress the number of organisms entering into the device, sensors configured to sense an entry of number of organisms into the device, and a processor communicatively coupled with the sensor and activates the fumigating agent based on the signal received from the sensor. The present disclosure also relates to method of trapping organisms.

Apparatuses and methods utilizing tactile transducers to create mechanical waves that travel through an individual's body to the kidneys to dislodge kidney stones. Embodiments include a structural member with at least one tactile transducer, an amplifier, and a controller. The tactile transducer(s) produce mechanical waves, and the structural member enables projection of the mechanical waves produced by the tactile transducer(s) toward at least one kidney to dislodge kidney stones. The amplifier is electronically coupled to the at least one tactile transducer, and the controller is electronically coupled to the amplifier and configured to determine the mechanical waves produced by the at least one tactile transducer.