Abstract: A wearable neurostimulator includes a fabric structure, a flexible circuit printed on the fabric structure with exposed electrically conductive portions, and a rigid PCB including an electrical circuit and exposed electrically conductive portions. A rivet includes a shank that extends through the fabric structure, conductive pads, PCB, and conductive vias. The rivet electrically connects the conductive portions of the PCB circuit to the conductive portions of the flexible circuit.

Abstract: An apparatus for applying electrical stimulation to a target peripheral nerve in a subject includes a wearable structure configured to be worn on at least one of the subject's lower leg, foot, or ankle. A first stimulation electrode is mounted on the wearable structure at a first location on the wearable structure. A second stimulation electrode is mounted on the wearable structure at a second location on the wearable structure, different than the first location on the wearable structure. One or more recording electrodes are mounted on the wearable structure. The apparatus also includes a control unit for controlling the operation of the first stimulation electrode, the second stimulation electrode, and the one or more recording electrodes. The wearable is configured to position the first stimulation electrode on a medial side of the target peripheral nerve, and to position the second stimulation electrode on a lateral side of the target peripheral nerve.

Abstract: A medical sling for supporting an anatomical feature having ends that are tapered using a folding fixture and then thermoset. The thermoset ends hold the bunched or folded shape thus allowing the ends to be removed from the fixture and placed into a mold assembly where anchors are molded over the ends.

Abstract: A medical sling for supporting an anatomical feature having ends that are tapered using a folding fixture and then thermoset. The thermoset ends hold the bunched or folded shape thus allowing the ends to be removed from the fixture and placed into a mold assembly where anchors are molded over the ends.

Abstract: A system and method for treating a medical condition of a subject and an apparatus for treating a medical condition of a subject by applying electrical stimulation to a target peripheral nerve. The apparatus includes a plurality of electrical stimulation electrodes are spaced from each other in a predetermined configuration and one or more recording electrodes. A wearable structure supports the stimulation electrodes and the recording electrodes spaced apart from each other. A control unit controls the operation of the stimulation electrodes and the recording electrodes. The control unit is configured to energize the stimulation electrodes to apply stimulation to a tibial nerve and record physiological response using the recording electrodes. The control unit is also configured to automatically detect the foot, right or left, upon which the apparatus is worn by monitoring a phase relationship or time delay between applying stimulation to the tibial nerve and recording the physiological response.

Abstract: A drive system for a tissue resection device that drives a cutting tube in a rotating and reciprocating motion simultaneously. The cutting tube moves within an outer tube having a window at a distal end thereof. When activation of the device ceases, the device remains powered until the cutting tube assumes an extended position, thereby closing the window.

Abstract: A medical sling for supporting an anatomical feature having ends that are tapered using a folding fixture and then thermoset. The thermoset ends hold the bunched or folded shape thus allowing the ends to be removed from the fixture and placed into a mold assembly where anchors are molded over the ends.

Abstract: Cochlear implant headpieces with improved moisture resistance.

Abstract: The present subject matter describes a suturing rings and method of manufacture of suturing rings for prosthetic heart valves. A plurality of suture holes are formed along a length of the metal sheet by performing punching or similar operations. The metal sheet has a substantially constant thickness throughout the length of the metal sheet. The rectangular metal sheet is rolled along the length until two ends of the metal sheet abut with each other. The two ends of the metal sheet are welded to form a metallic tube. The metallic tube is reshaping using a forming tool to obtain a suturing ring having an inner surface with a substantially convex profile. The suturing ring has an inner diameter at an inner peripheral edge at a first open end and an inner diameter at an inner peripheral edge at a second open end greater than an inner diameter at a mid-circumferential plane.

Abstract: A system includes a sound processor included in an electro-acoustic stimulation (“EAS”) device and that directs a cochlear implant to apply electrical stimulation to a patient and a receiver to apply acoustic stimulation to the patient. The system further includes a volume control facility and a selection facility that selectively associates the volume control facility with the electrical stimulation in response to a first user input, selectively associates the volume control facility with the acoustic stimulation in response to a second user input, and selectively associates the volume control facility with both the electrical stimulation and the acoustic stimulation in response to a third user input.

Abstract: Cochlear implant headpieces with improved moisture resistance.

Abstract: An exemplary system includes 1) an electro-acoustic stimulation (“EAS”) subsystem that directs a cochlear implant to apply electrical stimulation to a patient, and directs a receiver to apply acoustic stimulation to the patient; and 2) a volume control subsystem communicatively coupled to the EAS subsystem and that facilitates independent control of a first volume level perceived by the patient when the electrical stimulation is applied and a second volume level perceived by the patient when the acoustic stimulation is applied.

Abstract: An exemplary system includes 1) a first sound processor included in a first auditory prosthesis system associated with a first ear of a patient, the first sound processor including a first volume control facility, and 2) a second sound processor included in a second auditory prosthesis system associated with a second ear of the patient, the second sound processor including a second volume control facility. The first volume control facility adjusts, in response to actuation of the first volume control facility, a first volume level perceived by the patient when electrical stimulation is applied by either the first auditory prosthesis system or the second auditory prosthesis system. The second volume control facility adjusts, in response to actuation of the second volume control facility, a second volume level perceived by the patient when acoustic stimulation is applied by either the first auditory prosthesis system or the second auditory prosthesis system.

Abstract: An exemplary system includes 1) a first sound processor included in a first auditory prosthesis system associated with a first ear of a patient, the first sound processor including a first volume control facility, and 2) a second sound processor included in a second auditory prosthesis system associated with a second ear of the patient, the second sound processor including a second volume control facility. The first volume control facility adjusts, in response to actuation of the first volume control facility, a first volume level perceived by the patient when electrical stimulation is applied by either the first auditory prosthesis system or the second auditory prosthesis system. The second volume control facility adjusts, in response to actuation of the second volume control facility, a second volume level perceived by the patient when acoustic stimulation is applied by either the first auditory prosthesis system or the second auditory prosthesis system.

Abstract: A system includes a sound processor included in an electro-acoustic stimulation (“EAS”) device and that directs a cochlear implant to apply electrical stimulation to a patient and a receiver to apply acoustic stimulation to the patient. The system further includes a volume control facility and a selection facility that selectively associates the volume control facility with the electrical stimulation in response to a first user input, selectively associates the volume control facility with the acoustic stimulation in response to a second user input, and selectively associates the volume control facility with both the electrical stimulation and the acoustic stimulation in response to a third user input.

Abstract: An exemplary system includes 1) an electro-acoustic stimulation (“EAS”) subsystem that directs a cochlear implant to apply electrical stimulation to a patient, and directs a receiver to apply acoustic stimulation to the patient; and 2) a volume control subsystem communicatively coupled to the EAS subsystem and that facilitates independent control of a first volume level perceived by the patient when the electrical stimulation is applied and a second volume level perceived by the patient when the acoustic stimulation is applied.