Abstract: A massage device includes a coupling member adapted for attachment to a power output shaft, a proximal foam pad attached to the coupling member, and, a distal foam pad bottom. Portions of the distal foam pad are adapted to cover over at least one side of the proximal foam pad and form a highly resilient curved surface. A removable bonnet shaped and sized to tightly fit over the distal foam pad and proximal foam pad includes an outer surface with a low coefficient of friction that may be applied to over the clothing without grabbing for providing a softer and safer percussive massage.

Abstract: In at least one embodiment, a system and method for implanting an implantable medical device (IMD) within a patient may include an IMD including a housing and an attachment member, and a delivery catheter including a tethering snare that is configured to be selectively extended out of the delivery catheter and retracted into the delivery catheter. In at least one embodiment, a system and method for implanting an implantable medical device (IMD) within a patient may include an IMD including a housing and an attachment member, wherein the attachment member includes a central passage connected to a connection chamber, and a delivery catheter including first and second tethers that may be moved outwardly from and retracted into the delivery catheter.

Abstract: A tracheostoma valve to be applied to a tracheostomized person's neck comprises an air passage to be connected with the tracheostoma for connecting the trachea with the surroundings. A valve member is provided in the air passage, wherein the valve member is normally open and allows for inhalation and exhalation through the air passage. The valve further comprises a manually activated member for establishing an uninterrupted seal to block patient exhalation, thereby to direct it to the patient's pharynx, esophagus, sinuses, and mouth for speech following surgical removal of the larynx.

Abstract: A delivery catheter for a stent. The delivery catheter may comprise a distal end and a proximal end. The distal end includes a stent attachment region adapted to receive a stent. The stent may be of the self-expanding type. The catheter further comprises a handle at its proximal end and at least one sheath which may at least partially circumferentially cover said stent such as to retain it in a collapsed configuration. The sheath is coupled at its proximal end to an actuator located on said handle portion.

Abstract: A hybrid disposable face mask has a first mask section having a filter area sized and shaped to fit in overlapping relationship only about the mouth area of the wearer and a second mask section having inserts, one for each nostril, sized and shaped to be sealably retained air tight in each nostril. The second mask section can be linked to a valve assembly which opens during exhale and closes during inhale. The first mask section may be supported solely by the second mask section or by separate structure. The combination allows one to eat and drink while breathing through the nose filter.

Abstract: A medical device for sealing a defect in a body includes a wire frame that includes a plurality of wires that form a first occluding member and a second occluding member, the wire frame including a defect-occupying portion disposed between the first occluding member and the second occluding member. The defect-occupying portion is adapted to fill a wide range of potential defect sizes, such that no more than five devices of a range of sizes are required to effectively seal a range of nominal defect sizes of approximately 8 to 35 mm.

Abstract: The present invention is a motorized device used to apply pressure on a specific pressure point on a person's hand known to alleviate anxiety, pain, migraines, headaches and toothaches. The pressure point is located between the thumb and index finger in the web of the hand. The device consists of a motor and mechanism attached to two contact ends producing a circular motion while applying pressure to the specified pressure point. The mechanism is enclosed in ergonomic case suitable for use on both the left and right hand. Batteries are the source power.

Abstract: A respiratory pressure therapy (RPT) device is disclosed for treatment of respiratory-related disorders. The RPT device includes a pressure generator, a pneumatic block, a chassis and a device outlet for delivering a supply of flow of gas to a patient interface. The RPT device also comprises an integrated humidifier including a water reservoir. An RPT device is also disclosed that includes a wireless data communication interface integrated with the housing and configured to connect to another device or a network.

Abstract: An air inhalation device for insertion within the nostrils, comprising: at least one hollow frusto-conical tube member having an air passageway; a fan; a motor; and a power source; wherein the said frusto-conical tube has a forward end which tapers to form a rearward end, and is fitted with a power driven fan for enhancing the inhalation and exhalation of air.

Abstract: In an embodiment, a method is described. The method comprises obtaining an indication of a speech pattern of a subject and using the indication to determine a predicted time of inspiration by the subject. A machine learning model is used for predicting the relationship between the speech pattern and a breathing pattern of the subject. The machine learning model can then be used to determine the predicted time of inspiration by the subject. The method further comprises controlling delivery of gas to the subject based on the predicted time of inspiration by the subject.

Abstract: A humidifier includes a humidifier tub including an air inlet and an air outlet. The air outlet may have an exit port positioned in a plane disposed below the air inlet. A base plate is provided to the bottom of the humidifier tub. The base plate and humidifier tub define a water chamber adapted to receive a volume of water. The humidifier tub may include a guidance structure adapted to direct air entering the humidifier tub via the air inlet to swirl downwardly and around within the humidifier tub reaching the water surface before exiting the exit port. The tub may include a structure to prevent the inadvertent entry of water from the tub to the flow generator.

Abstract: A percutaneous valve delivery system may include an outer sheath and an inner catheter disposed within the outer sheath. The inner catheter may include a plurality of lumens formed therein. A tubular extension may extend distally from a distal end of the inner catheter, wherein the tubular extension is axially movable relative to the inner catheter. A nose cone may be attached to the tubular extension. A handle may be attached to the outer sheath, wherein the handle is configured to shift the outer sheath between a first position and a second position relative to the inner catheter. A valve replacement implant may be releasably coupled to the inner catheter.

Abstract: A subaxillary traction device having an elongated body portion with a first end and a second end, at least one receptacle member disposed on the first end defining a cavity to receive a fingertip, a handle opening disposed adjacent or near the first end and a handle opening disposed adjacent or near the second end, the handle openings being of sufficient size to receive at least one finger there through, whereby the body portion is positionable under the posterior axilla of a fetus experiencing shoulder dystocia such that traction may be applied allowing delivery of the posterior aim affecting the safe delivery of the baby.

Abstract: A Personal Protective Equipment that fits in the Nose of living species, especially human beings, this nose mask is designed for ease of use, comfort to the user, and most of all to filter harmful viruses, bacteria, other filterable microbes, dust particles, and prevent them from entering into their nostrils, thereby protecting the user and preventing them from contracting diseases such as but not limited to COVID-19 (largely known as the novel corona virus during the years 2019 to 2021 pandemic time period), while they are at work, outside, and/or indoors, to ensure that they lead a healthy life. Additionally this Personal Protective Nose Mask can be used for betterment of health by patients, under a Physician's care/treatment who are prescribed inhalable medicines.

Abstract: An expiratory limb is provided that is configured to remove humidified gases from a patient and configured to provide improved drying performance by providing a tailored temperature profile along the limb. Limbs for providing humidified gases to and/or removing humidified gases from a patient are also provided, the limbs having improved gas residence time at constant volumetric flow rate. The improved residence time can be achieved by providing a limb comprising multiple lumens.

Abstract: A folded expandable gastro-retentive device and its uses in human medical care include, inter alia, appetite suppression in a subject in need thereof. The expanded device can be included in kits.

Abstract: An invention to house a disposable dust mask or N95 mask in an independent comfortable and reusable face mask frame.

Abstract: A catheter mount is configured to be attached to a respiratory apparatus. The catheter mount includes a plurality of ports in fluid communication with each other. The plurality of ports include an interface port configured to connect to an interface tube, a conduit port configured to connect to a conduit tube, and at least one suction port configured to allow insertion of a suction catheter. The at least one suction port can be positioned to allow the suction catheter, when inserted, access to both the interface port and conduit port.

Abstract: Inflatable medical devices and methods for making and using the same are disclosed. The inflatable medical devices can be medical balloons. The balloons can be configured to have a through-lumen or no through-lumen and a wide variety of geometries. The device can have a high-strength, non-compliant, fiber-reinforced, multi-layered wall. The inflatable medical device can be used for angioplasty, kyphoplasty, percutaneous aortic valve replacement, or other procedures described herein.

Abstract: A system for assisting a rescuer with treatment of a patient is described. An example system includes a mobile computing device that includes a user interface and a processor coupled to memory. The processor is configured to cause the user interface to prompt the rescuer to select a proficiency level from among multiple proficiency levels including a basic proficiency level and at least one non-basic proficiency level. The basic proficiency level includes basic resuscitation instructions for the rescuer. The system is further configured to receive an input from the rescuer of the selected proficiency level. The system provides, if the rescuer selects the basic proficiency level, the basic resuscitation instructions to the rescuer, and provides, if the rescuer selects the at least one non-basic proficiency level, non-basic instructions to the rescuer. The system transmits signals to control a defibrillator according to the selected proficiency level.