The invention consists of an expansion catheter for intrauterine placement, featuring anatomical characteristics adaptable to the different morphologies of the uterine organ in its internal cavities, and which efficiently enables the dilatation and separation of the internal walls of the cavity subsequent to their reduction in the surgical process of endometrial scraping in the different surgical techniques of the procedure, in order to serve as a separator and isolator in the prevention of intrauterine adhesions, facilitating drainage both internally through the device and perimetrally. The device, containing an expansion device in a collapsed state, is placed in the uterus by means of an insertion device with the aid of a pusher, which is discarded together with the insertion device once the unit is in place.

A device for use with a uterine tamponade apparatus, such as the Bakri® postpartum hemorrhage balloon, is disclosed. The device comprises an anchor for deployment within the vagina to securely retain the balloon in its proper position within the uterine cavity, allowing the balloon to function as intended for the control and management of postpartum hemorrhage and uterine bleeding. Methods of use of the vaginal anchor are also disclosed.

The present invention comprises systems, methods and devices for the delivery of compositions for occluding or of means for opening conduits. The implantable occlusive material may be delivered pre-formed or in situ cured and, may be a resorbable material that supports tissue ingrowth that eventually replaces the material leaving little or no original material in place. The delivery system is positioned to allow for placement of the occlusive material into the body conduit. Use of delivery systems, methods and devices for re-opening an occluded body conduit are also included.

An end effector assembly of a tissue resection device. The end effector assembly including a first cut guide including a first support surface that extends from a first proximal end portion to a first distal end portion including a first outer distal portion, and a second cut guide located around the first cut guide. The second cut guide having a second support surface that extends from a second proximal end portion to a second distal end portion having a second outer distal portion. The first outer distal portion located distal of the second outer distal portion and the first outer distal portion being located farther laterally from the longitudinal axis than the second outer distal portion. The end effector assembly further including a cutting device located between the first and second cut guides.

A method and system of providing therapy to a patient's uterus. The system has an access tool with a lumen, the access tool being adapted to be inserted through a human cervical canal to place an opening of the lumen within a uterus when the access tool is inserted through the cervical canal; a seal disposed at a distal region of the access tool and adapted to seal the access tool against an interior cervical os; a sealing indicator adapted to provide a user with an indication that the seal has sealed the access tool with the interior cervical os; and a vapor delivery mechanism adapted to deliver condensable vapor through the access tool to the uterus, the condensable vapor being adapted to condense within the uterus.

The present invention comprises systems, methods and devices for the delivery of compositions for occluding or of means for opening conduits. The implantable occlusive material may be delivered pre-formed or in situ cured and, may be a resorbable material that supports tissue ingrowth that eventually replaces the material leaving little or no original material in place. The delivery system is positioned to allow for placement of the occlusive material into the body conduit. Use of delivery systems, methods and devices for re-opening an occluded body conduit are also included.

The present invention relates to a uterus manipulator in minimally invasive surgery that facilitates procedures of manipulation of the uterus, incising and suturing of all kinds of tissue connected to the uterus and particularly, incising the cervico-vaginal tissue in a circular line in laparoscopic hysterectomy, that prevents the incidence of various complications during said procedures, and that can be actuated (driven) manually without requiring any external energy source.

A device for retarding birth including an upper ring for surrounding a cervix, an anchoring component for anchoring the device, and an elastic component for attaching the upper ring to the anchoring component, wherein the elastic component pushes the upper ring and the anchoring component apart. A device for retarding birth including a sleeve for surrounding a cervix along a greater portion of a length of the cervix, a support strip on the sleeve directed along an axis of the sleeve, and a ring at least partially around the sleeve, in which when a top of the sleeve is pushed to expand radially, the support strip pivots on the ring, such that an end of the support strip near the top of the sleeve moves radially outward, and an end of the support strip near the bottom of the sleeve moves radially inward. Related apparatus and methods are also described.

An apparatus for use in a cerclage procedure includes a flexible support member and a plurality of compression members disposed along the flexible support member. Each of the compression members has a connecting feature through which a suture used during the cerclage procedure is passed. Each of the compression members transforms a radially-compressive force applied by the suture into a radial pressure applied against the cervix.

A cervical dilator including a stem comprising a partly or fully dehydrated hydrogel comprising a water-insoluble synthetic hydrophilic polymer capable of radial expansion due to absorption of water from a bodily fluid. The cervical dilator softens and ripens the cervical tissue and expands the cervical canal by a combined action of radial hydrogel stem expansion and osmotic withdrawal of water from the tissue. The osmotic withdrawal is caused by at least one osmotically active compound, such as a water-soluble salt, a polyelectrolyte, or a mixture thereof, wherein the at least one osmotically active compound is dispersed in the hydrogel. The cervical dilator may also include a non-toxic plasticizer of the hydrogel, such as water.