Disclosed herein are sealing devices configured for improving sealing functionality with an engaged extension member of an apparatus. More specifically, disclosed herein are trocar sealing devices configured for improving insufflation gas containment in relation to trocars (and/or other related type of devices) that are used for enabling a surgical instrument such, for example, a laparoscope, to gain access to an abdominal cavity (or other body cavity). By providing for such improved insufflation gas containment, sealing devices as disclosed herein are particularly advantageous, desirable and useful in view of long-standing reasons for limiting insufflation gas leakage and in view of newly recognized reasons stemming from outbreak of COVID-19 disease for limiting insufflation gas leakage.

In some embodiments an apparatus for providing access for a medical procedure in a patient's body cavity includes a stem configured for insertion through an opening in a body cavity wall. The stem has a bore and a cap is disposed at a proximal end thereof and includes an entry port in communication with the bore which receives an instrument to be inserted into the body cavity. An inflatable annular seal is disposed on the stem proximate the cap and a conduit extends through the cap providing pressurized gas at a first outlet in fluid communication with the body cavity providing insufflation pressure. A second outlet of the conduit is in fluid communication the seal, which when disposed inside the body cavity proximate the wall and inflated by pressurized gas, bears on an inner surface of the wall urging the cap into contact with an outer surface of the wall while sealing the opening.

A single-port surgical device includes a housing and one or more cannulas. The housing includes a proximal port and a distal port, the one or more cannulas include an inner cannula section and an outer cannula section, the inner cannula section is located in the housing and communicates with the distal port of the housing, the outer cannula section is located outside the proximal port of the housing, and at least a portion of the outer cannula section of at least one cannula of the one or more cannulas is deformable in a radial direction, an axial direction or the radial direction and the axial direction of the outer cannula section.

A method for implanting a replacement heart valve within a diseased valve includes accessing a patient's heart by piercing a myocardium, advancing a guidewire into the patient's heart, and installing an access device in a wall of the heart. The access device preferably has at least one valve mechanism. A valve delivery device is advanced over the guidewire and through the access device. The valve delivery device has a replacement heart valve disposed along a distal end portion thereof. The replacement heart valve preferably includes an outer support structure and a leaflet valve disposed within the outer support structure. The replacement heart valve is radially expanded within the diseased valve. During implantation, the outer support structure conforms to a diameter of the diseased valve and the leaflet valve expands to a fixed size having a diameter smaller than the diameter of the diseased valve.

A suture delivery system is described. The system includes an anchor and a cooperating driver, the driver facilitating a delivery of the anchor into the abdominal cavity. The system allows for the deployment of a suture internally into an abdominal wall.

A trocar surgical seal or surgical access device is provided. The trocar surgical seal comprises first and second supports coupled together by a film passageway. The trocar surgical seal provides an instrument seal for instruments inserted therethrough. The trocar surgical seal occupies minimal surgical space.

A surgical access device has a cannula tube with a collar coupled to a proximal region of the cannula tube. A balloon is attached to the cannula tube. The collar includes a receptacle and an inflater is insertable into the receptacle. The inflater has a body with a chamber and a first compound. A cap is attached to one end of the body and has a cavity containing a second compound. A membrane is disposed between the body and the cap and is configured to keep the first and second compounds separate. A button extends through an opening of the cap and a piston is coupled to the button. The piston includes a spike extending away from the button and is translatable in the cap between a rest position and an actuated position. The actuated position is defined by a portion of the spike penetrating the membrane such that the first compound interacts with the second compound generating a gas that is communicated to the balloon via a groove of the cannula tube.

An attachment (1) for a trocar cannula (3) having an access valve (12) located in a proximal end (5) thereof comprises a housing (20) defining an instrument passageway (29). An operating member (43) having an instrument bore (46) is slideable in the instrument passageway (29) from a disengaged state disengaged from the access valve (12) to an engagement state extending through the access valve (12) with the access valve (12) in the open state and shielded from an instrument passing therethrough. A pair of detecting probes (55) carried on a carrier (50) and extending into the instrument bore (46) are urgeable distally from a first state to a second state by a distal end of an instrument being urged distally in the instrument bore (46) for in turn urging the operating member (43) from the disengaged state to the engagement state. A proximal seal (40) in the instrument passageway (29) is urged from a non-sealing state to a sealing state by the operating member (43) being urged from the disengaged state to the engagement state.

A pad is provided having a body for providing a gas seal over a surgical site, a port extending between a first surface of the body and a second surface of the body and sized accept a surgical instrument, and a lumen situated along the body and having a first opening and a second opening, the second opening aligned with the surgical site for communicating a fluid flow to the surgical site.

A probe may be inserted into a body cavity to perform diagnostic intervention(s), therapeutic intervention(s), or both. The probe may be inserted through a body aperture that is naturally occurring or man-made, intentionally or by accident. The body aperture may form a seal encircling the probe so that insufflation retention material may be effectively retained in the body cavity so that an operator can perform the intervention(s). However, there may be leakage of the insufflation material. The insufflation retention device is configured to form an effective seal contactingly adjacent the body aperture and to provide a passageway for the introduction of the probe into the body cavity, such that a diagnostic intervention or therapeutic intervention or both may be performed.