Splints for diagnostic and/or therapeutic purposes are disclosed. In one aspect, the present disclosure relates to a splint system for diagnostic and/or therapeutic functions for a patient with a vascular impairment. In one embodiment, the splint system includes a splint having: a leg supporting portion and a foot supporting portion, that are configured to support and secure the leg and foot of the patient; a locally and/or remotely controllable portion for setting a dorsiflexion angle of the foot of the patient, including electrical and/or mechanical controls and one or more actuators for setting of the dorsiflexion angle, for providing treatment to improve vascular function; and a plurality of physiological parameter sensors for measuring physiological parameters of the leg and/or foot of the patient, wherein the physiological parameters are associated with vascular function in the leg and/or foot of the patient.

Systems and methods for applying enhanced guided active compression decompression cardiopulmonary resuscitation are provided. Exemplary systems include a load cell, a handle, an adhesive pad. The handle and the adhesive pad are configured for magnetic coupling.

A wearable device measures, tracks, and monitors a wearer's physical physiological conditions during a rehabilitation period. Metrics such as temperature, patellar shifting, limb circumference, and acceleration may be collected. Changes in monitored conditions may be assessed for detecting medical abnormalities which require specialized attention, including for example embolisms or infections. A networked communication system and various user interfaces may be used for medical support personnel and patients alike to stay updated with the patient's rehabilitation progress and to make adjustments in a patient's individual rehabilitation program.

A multifunctional cardiopulmonary resuscitation machinery equipment may include a first-aid kit body, and a pressing device, a ventilation device, a monitoring device, a defibrillation device and a control device which are installed on the first-aid kit body; the upper end surface of the first-aid kit body is concavely provided with a curved pillow opening; a belt is counter-pulled between the edges of both sides of the inner side surface of the protecting pad; the pressing device and the defibrillation device are integrated and sleeved on the belt; the ventilation device comprises an oxygen generation pump, an oxygen mask and a gas transmission pipe which are integrated inside the first-aid kit body, and an output port of the oxygen generation pump penetrates through the first-aid kit body and is connected with the oxygen mask.

A blood flow stimulating device comprising: a boot (101) including a sole (111) and an upper; a sock (11) disposed within the boot (101): and a bladder (19) disposed within or on the sock (11), wherein the bladder (19) is configured to undergo repeated inflation and deflation so as to stimulate blood flow in a wearer of the blood flow stimulating device, wherein the sock (11) further includes a toe region (1002), a heel region (1001) and a raised portion (1003) between the toe region (1002) and the heel region that (1001), in use, reduces the distance between the sock (11) and a foot of a wearer of the blood flow stimulating device at the raised portion of the sock.

Systems and methods for interactive treatments of female sexual disorders are presented. A programmable sexual stimulation device is provided, which transmits and receives data relating to the use and function of the device. The sexual stimulation device may be programmed to implement a particular combination of mechanical actions which have been customized by a user or a health care professional involved in the treatment or preference of the user. The device may also collect data on the type of mechanical actions input by the user and transmit the data to a remote location for viewing by the user or the healthcare professional. The device may also communicate with external devices which aid in the treatment programs, such as audio or image display devices which can coordinate the function of the sexual stimulation device with the presentation of audio or visual information to provide additional sources of sexual arousal to the user.

A device for massage and applying a cosmetic product includes a structure having a contact face and a handling face. On the contact face of the structure, a pair of notched rollers that are free to rotate about concurrent axes is provided. The device includes an elastic suspender for the notched rollers with respect to the structure. On the handling face of the structure, on the opposite side from the contact face, the device includes a gripping form in the form of a spherical cap enveloping the surface of the structure.

The disclosure provides a fit-check device and associated methods. In some embodiments, the device may be used in conjunction with a rigid or semi-rigid partially circumferential concussion-mitigating collar to determine whether the collar is appropriately sized for the user and is applying the desired amount of force to the neck veins.

A wearable device measures, tracks, and monitors a wearer's physical physiological conditions during a rehabilitation period. Metrics such as temperature, patellar shifting, limb circumference, and acceleration may be collected. Changes in monitored conditions may be assessed for detecting medical abnormalities which require specialized attention, including for example embolisms or infections. A networked communication system and various user interfaces may be used for medical support personnel and patients alike to stay updated with the patient's rehabilitation progress and to make adjustments in a patient's individual rehabilitation program.

A prosthetic penis provides the wearer with somatosensory feedback on another part of the wearer in response to external influences or stimuli on the prosthetic penis. Sensors on the prosthetic penis are mapped to output elements on an output device that is in contact with the wearer's body. The output device may be applied to the wearer's skin or inserted anally or vaginally. Feedback of touch, pressure, and/or temperature on the prosthesis is such that the wearer's perception mimics that of touch, pressure, and/or temperature stimuli on an actual, biological penis.