A vaginal ring sensor device adapted to be placed within the vaginal vault of a user, the device including a ring body, at least one through hole that passes through the ring body, and at least one biosensor structured and arranged to sense and/or measure a parameter of vaginal fluid as such fluid passes through the at least one through hole.

An apparatus includes a shaft having a proximal end and a distal end; a stem extending from the distal end of the shaft and comprising a first cover and a second cover, the first cover and the second cover being configured to inhibit access to fallopian tubes of a patient; and a plurality of temperature sensors disposed on the shaft and on the stem. At least one of the temperature sensors is positioned between the proximal end of the shaft and the distal end of the shaft and at least one of the temperature sensors is positioned on the stem.

Absorbent articles with biodegradable and/or biocompostable elements are disclosed, wherein the absorbent articles include sensors. The sensors detect and determine variables associated with collected fluids, solids, and gases, including a presence of fluids, solids, and gases, a volume of fluids, solids, and gases, and/or a distribution of fluids, solids, and gases. In one embodiment, the sensors and/or connected computing systems are calibrated to capacities and other properties of elements within the articles, including superabsorbent polymers, and are operable to trigger an alert based on detected or determined conditions.

A method of assessing Fallopian tubal patency includes introducing a distension medium into a patient's uterus, introducing a contrasting medium into the uterus, and observing the contrasting medium, for example, via a hysteroscope, to determine whether the contrasting medium flows into one or both Fallopian tubes. A device for assessing Fallopian tubal patency includes a chamber for receiving contrast media, a flow path through the chamber for delivering distension media to a patient's uterus, and a flow controller for regulating the flow of distension media to the patient's uterus. The flow path is configured to permit flow of contrast media from the chamber into the flow path.

A method, system, device and computer program product for analyzing absorbent articles (300) are provided. The method includes receiving an image or data representing an image of an absorbent region (302) of an absorbent article. The absorbent region comprises at least one stain (350) caused by a bodily fluid discharge of a person using the absorbent article. The absorbent region includes at least one reference mark (304). A surface area of the stain (350) is computed using the at least one reference mark (304). The computed surface area of the stain (350) is used to determine a volume of bodily fluid contained in the absorbent article (300). The volume of the bodily fluid is analyzed to assess a measure of the bodily fluid discharge of the person.

Featured are intravaginal devices and electrical stimulation devices, systems, thereof, and methods of using the devices and systems thereof to observe pelvic floor movements in order to diagnose, treat, or prevent urinary and fecal incontinence disorders (e.g., urge incontinence) and their accompanying symptoms or to diagnose and/or improve the efficacy of neuromodulation therapy.

Introduced here is technology to monitor moisture levels in a hygiene product, such as tampons, pads, menstrual cups, child diapers, adult diapers etc. According to one embodiment, a moisture sensor is inserted inside a feminine hygiene product. The moisture sensor is connected to a wearable device that gathers the moisture data and sends the data to a mobile device, such as a cell phone. The cell phone generates notifications to the user, such as percentage saturation of the feminine hygiene product, message to change the feminine hygiene product, expected start and end dates of the next menstrual cycle, etc. According to another embodiment, the moisture sensor can be inserted in other hygiene products, such as child diapers or adult diapers, to measure the amount of urination, defecation, or other excretions, and to generate notifications to the user, the user's caretaker, or a third party.

A computer implemented method and system are provided. Such a method includes collecting health data from a female subject, assessing hormonal irregularities based on the health data to identify a pattern of hormonal imbalance, and prescribing a personalized herbal formula based on the pattern of hormonal imbalance to prevent or treat a condition or disorder related to a menstrual cycle of the female subject. Health data, which may be collected through online assessment, may include self-reported answers to a list of questions, and one or more photos of tongue of the female subject.

Methods of enhancing reproductive capacity in a female subject are provided. Aspects of the methods include inducing infertility in the subject in a manner effective to cause the subject to mount a compensatory response and thereby enhance reproductive capacity in the subject. Systems and kits useful in practicing the methods of the present disclosure are also provided.

A method of assessing Fallopian tubal patency includes introducing a distension medium into a patient's uterus, introducing a contrasting medium into the uterus, and observing the contrasting medium, for example, via a hysteroscope, to determine whether the contrasting medium flows into one or both Fallopian tubes. A device for assessing Fallopian tubal patency includes a chamber for receiving contrast media, a flow path through the chamber for delivering distension media to a patient's uterus, and a flow controller for regulating the flow of distension media to the patient's uterus. The flow path is configured to permit flow of contrast media from the chamber into the flow path.