A robotic assembly control system is disclosed. The robotic assembly control system includes an exoskeleton apparatus adapted to be worn by a user, at least one robotic assembly, the at least one robotic assembly controlled by the user by way of the exoskeleton, and at least one mobile platform, the at least one mobile platform controlled by the user and wherein the at least one robotic assembly is attached to the at least one mobile platform.

In one aspect, an obesity treatment device includes multiple inflatable space-filling compartments and a valve system for introducing fluid into each compartment, where the device forms, upon filing the compartments, to a curved shape conforming to a natural three-dimensional kidney shape of the stomach. In one aspect, a method for deploying a gastric balloon structure in a gastric cavity includes determining dimensions of the gastric cavity in a feeding state, selecting a fill volume for each of a number of isolated chambers of the balloon structure, and filling each chamber while the balloon structure is in the gastric cavity. In one aspect, a system for treating obesity includes a means for conforming a flexible, space-filling structure to a natural kidney shape of the gastric cavity, a means for maintaining at least two isolated inflatable regions of the flexible, space-filling structure, and a means for introducing fluid into each inflatable region.

The present disclosure provides alert implants that comprise a medical device and an implantable reporting processor (IRP), where one example of such a medical device includes a component for a total knee arthroplasty (TKA) such as a tibial extension, a femoral component for hip replacements, a breast implant, a distal rod for arm or leg breakage repair, a scoliosis rod, a dynamic hip screw, a spinal interbody spacer, and tooling and methods that may be used to form the alert implant, and uses of such alert implants in the health maintenance of patients who receive the implant.

A prosthetic arm apparatus including a plurality of segments that provide a user of the prosthetic arm apparatus with substantially the same movement capability and function as a human arm. The segments are connectable to one another and connectable to a prosthetic support apparatus that may be adorned by the user. A prosthetic limb segment includes a housing having an input interface and an output interface, the output interface and the input interface being moveable with respect to one another, a motorized drive disposed within the housing, the motorized drive effecting movement of at least one of the output interface or the input interface, and a controller disposed within the housing for controlling actuation of the motorized drive. The controller may be configured to communicate with at least a second motorized drive of at least a second prosthetic limb segment to control actuation thereof.

A biomedical implant includes a wall enclosing at least a portion of the implant. The wall includes a first stratum and a second stratum conformal with the first stratum. An interlayer is provided between the first and the second strata, and includes a structure that produces capillary pressure in an infiltrating fluid in response to rupture of the first stratum or the second stratum resulting in entry of the infiltrating fluid into the interlayer. A detector is exposed to the interlayer and configured to detect a presence, if any, of the infiltrating fluid and output a detection state indicator. A communication circuit is communicatively coupled to the detector and configured to communicate the detection state indicator to a reader external to the patient.

The present disclosure provides alert implants that comprise a medical device and an implantable reporting processor (IRP), where one example of such a medical device includes a component for a total knee arthroplasty (TKA) such as a tibial extension, a femoral component for hip replacements, a breast implant, a distal rod for arm or leg breakage repair, a scoliosis rod, a dynamic hip screw, a spinal interbody spacer, and tooling and methods that may be used to form the alert implant, and uses of such alert implants in the health maintenance of patients who receive the implant.

A system can include an aural computing system in communication with the ophthalmic device. In some embodiments, the aural computing system can include a wireless communication device in communication with the ophthalmic device. In some embodiments, the ophthalmic device comprises a contact lens, which can inserted into the user's eye. The wireless communication device can comprise wearable technology.

A method is provided for rerouting flow through the small intestine of a patient with an implanted artificial sphincter that encircles a portion of the small intestine. The small intestine includes a duodenum, a jejunum extending from the duodenum, and an ileum extending from the jejunum. The method includes providing the artificial sphincter in an open state to thereby permit intestinal flow through the encircled portion of the small intestine such that the intestinal flow passes through the duodenum, the jejunum, and the ileum. The method further includes, in response to a user-activated electrical input, transitioning the artificial sphincter to a closed state to constrict the encircled portion of the small intestine and thereby redirect intestinal flow from a first portion of the small intestine to a second portion of the small intestine such that the intestinal flow bypasses at least a portion of the jejunum.

A robotic assembly control system is disclosed. The robotic assembly control system includes an exoskeleton apparatus adapted to be worn by a user, at least one robotic assembly, the at least one robotic assembly controlled by the user by way of the exoskeleton, and at least one mobile platform, the at least one mobile platform controlled by the user and wherein the at least one robotic assembly is attached to the at least one mobile platform.

A system for powering a prosthetic arm is disclosed. The system includes at least one internal battery located in the prosthetic arm, at least one external battery connected to the prosthetic arm, and a master controller configured to connect either the at least one internal battery or the at least one external battery to a power bus to power the prosthetic arm.