The present disclosure relates to an insertion type drug injection device capable of being inserted into a body for injecting a drug into a skin, including: a main body having an open insert part and formed in a tubular shape having a hollow space therein, a needle assembly formed in the insert part, provided with a plurality of needles, and including a pneumatic port and a drug injection port, and a drug injection pipe inserted into the main body and connected to a drug injection port of the needle assembly, and an air flowing pipe connected to the pneumatic port.

The invention relates to a neovaginal prosthesis formed by an essentially cylindrical hollow main body comprising a closed upper end and an open lower end, and a securing plate intended to connect to the lower end of the main body.

One aspect of the invention provides a vaginal stent system including: an inflatable vaginal stent and a removable handle. The inflatable vaginal stent include includes: an elastomeric exterior wall and a first fitting located at a base of the inflatable vaginal stent. The removable handle is adapted and configured for insertion, inflation, and removal of the inflatable vaginal stent from a subject's vagina. The removable handle includes a second fitting complementary to the first fitting and adapted and configure to form substantially fluid tight coupling when the handle is coupled to the inflatable vaginal stent. Another aspect of the invention provides a method of fabricating a customized vaginal stent or dilator. The method includes: generating a 3D model of a vaginal stent or dilator; and controlling a 3D printer to fabricate a vaginal stent or dilator according to the 3D model.

The present disclosure generally relates to an applicator for administering a composition for treating one or more of vaginal dryness, vaginal irritation, vaginal itch, vaginal infection, vaginal odor, vaginal chafing, dyspareunia, and/or vaginal atrophy, and more specifically, to an applicator comprising a receptacle comprising a first portion, a second portion, and an attachment structure, where the first portion and second portion are removably attached to define a substantially spherical shape, where a vaginal care composition is stored within the receptacle.

A girth adjustable device for dilation and stretch of body orifices for medical applications, massage, body orifice improvement and activities pleasurable to the body, that can repeatedly, gradually increase and decrease a uniform and sustainable pressure against the entire lateral surface area of body orifices. The girth adjustable device comprises at least one controller, a housing, at least one threaded shaft, at least one module, a plurality of shaft members and at least one sheath. The part of the girth adjustable device that has to be inserted into body orifices is the shaft. In a body orifice, the user increases and decreases the girth size of the shaft via the controller.

An applicator 270 includes a stem 174 having an axially-formed slot delivery passage 200. A slot 350 is formed transaxially through the stem 174 and is in communication with the slot delivery passage 200. An extended side wall 350b is formed on one side of the slot 350. A flat surface 354, which is formed in the stem 174, is spaced and extends angularly away from an opposite side of the slot 176 and from the extended side wall 350b to provide for direct and lateral dispensing of a cream 280 onto a tissue 242 of a patient.

A pessary for the prevention of preterm birth, and in particular two pathological conditions of pregnancy known as isthmico-cervical incontinence and cervical shortening, both of which are associated with increased risks for pregnancy loss and/or premature deliveries of babies. The pessary includes a sleeve supported within a ring by an annular member. The sleeve is intended to contact the cervix and maximize the length of the cervix while the annular member and ring contact the vagina. The pessary may be fabricated from a pliable medical-grade silicon, and the pessary may include one or more sensors to measure various patient parameters indicative of a premature cervical contraction.

A portable device (500) for examining a body cavity, the device (500) adapted to allow air to be introduced into the body cavity, the device comprising: a tubular probe (1) having a first, forward end (4) and a second, rearward end (5); and a sealing element (506) disposed adjacent to the forward end (4) of the tubular probe (1), the sealing element (506) including a self-tightening sleeve portion (508) to engage the tubular probe (1), the sealing element (506) adapted to act as a seal for the body cavity to reduce egress of fluid therefrom by sealing against a circumferential zone of the internal tissue defining an orifice of the body cavity, the tubular probe (1) having a first lateral entry port (14) that allows for an elongate implement to be removably mounted in the device (500) and to be passed through the tubular probe (1) for introduction into the body cavity, such that the implement is manipulable by a user, the portable device (500) being connectable to an odour evacuation system having a filter (56) to remove the build-up of air in the body cavity, and wherein fluid being introduced into said body cavity via the tubular probe (1) is delivered via a conduit (51) from a pump (52), and a regulator (54) fluidly connected to the conduit (51) regulates the fluid to be within at least one predetermined range of pressure between at least an upper limit and a lower limit.

Methods and devices to affect types, proportion, quantity, distribution, or proliferation of microorganisms within a female reproductive system.

Set of applicators for dispensing topical products in a single dose in the anal, oral, rectal, vaginal and vulvar mucous and semi-mucous membranes. The encasement type packaging is similar to a condom, but smaller, presenting a compartment filled with the desired pharmaceutical formulation to be used in a single dose, located at its distal end, which contains orifices through which the product will be expelled. The content of the packaging can be applied with the finger of an individual or with a portable applicator. Said portable applicator does not directly contact the mucous and semi-mucous membranes, since it is covered by the fine encasement. The applicator has two encasable parts, making the transport thereof efficient, since it is extended upon encasement. A rounded anatomic part is encased in the applicator for compressing the product reservoir. The solution developed can be used to deliver medications to treat medical conditions and illnesses, or promote relief and comfort, in a safe, efficient, practical and discrete manner.