A multifunctional pill box carrying pouch is revealed. The pill box carrying pouch includes at least one pill box, at least one pouch, and at least two long ties. The pill box is a rigid rectangular box while the two long ties form a single longer tie. The respective long ties are detachably connected to the pouch by the two second connecting members. The pill box carrying pouch has a limb-carrying mode and a waist-carrying mode. Users can select the limb-carrying mode of the pill box carrying pouch when user's limb is injured and a support for the limb is required. By the two long ties arranged adjacent to each other and tightened around an arm or a leg of the human body, the pill box carrying pouch is closely attached to the wound on the limb for supporting wounded area or for hemostasis.

An anatomical gripping system comprising: a binding comprising: a substantially rigid spine; a calf shell mounted to the substantially rigid spine; an anterior shell; and a clamping mechanism connecting the anterior shell to the calf shell; wherein the calf shell comprises a flexible portion configured to selectively engage the superior portion of the calcaneus bone of a patient; and further wherein when the clamping mechanism applies a force to the flexible portion of the calf shell, the flexible portion of the calf shell is drawn into engagement with the superior portion of the calcaneus bone of the patient.

An orthopaedic device with a shell mechanism which can be brought into a closed position in which it engages at least partially around a body part arranged in the shell mechanism, and into an open position, in which the body part can be brought into the shell mechanism, wherein the shell mechanism can be brought from the open position to the closed position by means of the body part being introduced into the shell mechanism. The device has at least one actuation element which is arranged and designed in such a way that it is actuated when the body part is introduced into the shell mechanism, and it brings the shell mechanism from the open position to the closed position, wherein the actuation element has a tensile force transmission element, in particular a band or a cloth.

An exoskeleton wear management method is provided. The method includes receiving inertial data from a sensing system; determining whether a left leg component of an exoskeleton device is parallel to a left leg of a user and a right leg component of the exoskeleton device is parallel to a right leg of the user according to the received inertial data; in response to determining that the left leg component/the right leg component is not parallel to the left leg/the right leg of the user, prompting an adjusting left leg component message/an adjusting right leg component message; and in response to determining that the left leg component is parallel to the left leg of the user and the right leg component is parallel to the right leg of the user, prompting a left leg component and right leg component correctly-worn message.

An anatomical gripping system comprising: a binding comprising: a substantially rigid spine; a calf shell mounted to the substantially rigid spine; an anterior shell; and a clamping mechanism connecting the anterior shell to the calf shell; wherein the calf shell comprises a flexible portion configured to selectively engage the superior portion of the calcaneus bone of a patient; and further wherein when the clamping mechanism applies a force to the flexible portion of the calf shell, the flexible portion of the calf shell is drawn into engagement with the superior portion of the calcaneus bone of the patient.

A method and system for creating a custom-fit orthopedic cast comprises obtaining at least one measurements taken from at least one image of a body part, selecting a template cast, modifying the template cast according to the measurements taken from the at least one image to generate a custom cast model and rendering a custom cast based on the custom cast model.

Systems for immobilizing a patient are disclosed. The system includes at least one preform formed from a low melting temperature thermoplastic, the preform being configured to be formed to the anatomy of the patient, at least one frame coupled to the at least one preform, and at least one support configured to support the anatomy of the patient. The system also includes at least one lock mechanism coupled to at least one of the frame and the support and configured to couple the at least one frame to the at least one support, and at least one adjuster mechanism coupled to at least one of the at least one frame and the at least one support and configured to selectively adjust a distance between the at least one frame and the at least one support while the at least one frame is coupled to the at least one support.

Systems for immobilizing a patient are disclosed. The system includes at least one preform formed from a low melting temperature thermoplastic, the preform being configured to be formed to the anatomy of the patient, at least one frame coupled to the at least one preform, and at least one support configured to support the anatomy of the patient. The system also includes at least one lock mechanism coupled to at least one of the frame and the support and configured to couple the at least one frame to the at least one support, and at least one adjuster mechanism coupled to at least one of the at least one frame and the at least one support and configured to selectively adjust a distance between the at least one frame and the at least one support while the at least one frame is coupled to the at least one support.

A splint may be used to support or immobilize a body portion of a patient. Some splints may include one or more features to facilitate transport, placement, and/or manipulation of a splint. For example, some splints may be relatively lightweight, rugged, and in a compact configuration prior to use. Some splints may use radiolucent materials to permit x-ray examination of the relevant appendage without removal of the splint. Some splints may be used with other accessories or devices to facilitate immobilization of a limb and/or transport of the injured individual.

Usage of the Original Device Broken Down: The original device was created to stabilize a unilateral (one leg) closed mid shaft femur fracture by the use of held in place mechanical traction. The device has parallel telescoping rails, made from the frame itself, these rails allow the device to be adjusted and size appropriate for all heights of patients requiring this device. These rails lock in the position the medical provider deems correct. To start the application process, a medically trained individual must first apply an ankle brace (if no ankle fracture is present) to the injured leg, this brace has a loop attached to the bottom of it (this loop is used later), the provider will then pull manual traction using the ankle of the injured leg in a directional manner meant to realign the broken femur to its normal position prior to the break. The goal is to stretch the shortened injured leg until it meets the length of the non-injured leg. The force needed to reach this position is then matched by the devices mechanical ability to recreate the same amount of force the provider used to hold the leg in proper place. The original device then uses a strap that wraps around the whole upper portion of the injured leg (ischium/groin/thigh area), this strap secures the upper leg to the device and now becomes the anchor point the device will use to pull traction against. After this groin strap is secured, the device has a ratchet strap that can now be attached to the ankle brace loop mentioned above. Traction is now applied by pulling the leg taught until it matches the manual force applied by the provider; this is done by using a hand turned dial located on the device end. Once the desired outcome is reached, the device is then secured in place to inhibit any further movement until further medical care is required.

Usage of the Modified BTSD Broken Down: The BTSD will serve the same function as the original, being a tool that is specific for a unilateral closed mid shaft femur fracture; but will also come optional to be outfitted with two fixed in place ratchet assemblies for treating a bilateral femur fracture. The key differences the BTSD will have over the original will be (1) better overall stabilization to the injured leg, (2) the BTSD design change to the original frame offers a simpler and a more practical application which now allows the uninjured leg to be part of stabilization process, (3) the BTSD offers a less painful, more effective and overall safer means of traction being applied, (4) the BTSD ratchet assembly housing will come optional with one ratchet strap housing assembly being able to slide and lock into grooved/notched positions found on