A medical device can include a housing, a first seal structure, and a seal expander. The first seal structure can have a proximal end and a distal end, and a side wall surrounding and defining an interior chamber. A seal wall can be connected to the side wall and include an expandable opening. A seal expander can be coupled to the housing, and can be at least partially in the interior chamber of the first seal structure. The seal expander can include an expandable neck portion and a seal interface portion, the seal interface portion being near an intersection of the side wall and the seal wall.

A thermal pad for controlling a patient's temperature includes first and second chambers defined between interior and exterior layers. The first chamber circulates a temperature controlled fluid from a first inlet to a first outlet. The second chamber is in fluid communication with a port and a plurality of holes defined in the interior layer. Pressurized gas supplied to the second chamber is vented onto the patient to control the microclimate between the patient's skin and the thermal pad. An additional third chamber is provided in some embodiments that urges the thermal pad into contact with the patient when subjected to negative gauge pressure. In other embodiments, a negative gauge pressure chamber is allowed to partially inflate in order to urge the thermal pad into contact with the patient.

Various surgical systems are disclosed. A surgical system can include a surgical robot and a surgical hub. The surgical robot can include a control unit in signal communication with a control console and a robotic tool. The surgical hub can include a display. The surgical hub can be in signal communication with the control unit. A facility can include a plurality of surgical hubs that communicate data from the surgical robots to a primary server. To alleviate bandwidth competition among the surgical hubs, the surgical hubs can include prioritization protocols for collecting, storing, and/or communicating data to the primary server.

Implants comprising electrically-responsive hydrogel are described. Systems to provide electricity to induce response in hydrogel-containing implants are described. Methods for utilizing said system and methods for utilizing said hydrogel-containing implants are described.

An insufflator for exposing structures within an internal cavity forming a confined volume within an animal or human body, the apparatus including: an input conduit for exchanging gas with the confined volume; a gas insufflator for insufflation of gas into the confined volume through the input conduit, wherein the gas insufflator is configured to deliver an insufflator pressure to the confined volume, wherein the gas insufflator is configured to (super)impose at least one pressure or flow oscillation to obtain a forced oscillating pressure or flow delivered to the confined volume, the forced oscillating pressure or flow having at least one component with a frequency and an amplitude; a monitoring unit for monitoring a response of the internal cavity to the forced oscillating pressure or flow for determining one or more physical properties of the internal cavity; and an adapter unit for adjusting the insufflation pressure based on the determined one or more physical properties of the internal cavity.

Method and apparatuses for providing access to a body cavity of a living animal through an access port inserted in an incision made in a wall of the body cavity are disclosed. In some embodiments, the apparatus includes a cap configured to attach to the access port, the cap including an opening configured to permit insertion of a medical instrument through the cap and access port into the body cavity, and a tubular sleeve including a distal end sealingly connected at the opening and extending outwardly therefrom, the sleeve including a proximal end configured to receive and provide a seal with the medical instrument when received. The apparatus also includes a closure disposed to temporarily seal the sleeve prior to insertion of the medical instrument through the opening in the cap.

A surgical access device including a housing having a nozzle assembly, a gas supply plenum, a gas return plenum, and a pressure sensing plenum, as well as an elongated tubular body that extends from the housing portion and defines a central lumen communicating with the nozzle assembly and the gas return plenum, a telescopic cannula assembly associated with the tubular body and including a proximal section arranged coaxially within the tubular body and a distal section coaxially supported within the proximal section and mounted for movement relative to the proximal section between retracted and extended positions, and an elastomeric sheath associated with the telescopic cannula assembly and having a distal anchor portion for securing the surgical access device during a laparoscopic surgical procedure.

Embodiments of the present disclosure provide an apparatus and method for reducing surgical smoke. An exemplary apparatus includes trocar comprising a tubular hollow body circumscribing a cavity extending through a longitudinal axis of the trocar with a gasket at a first end and an exit port at a second end, the tubular hollow body comprising a first wall circumscribing the cavity and a concentrically spaced apart second wall. The apparatus further includes a first plate operable to maintain an electric charged disposed within the cavity on the first wall, and a second plate operable to maintain an electric charge disposed between the first wall and the spaced apart second wall.

System and method for modification of fluid environment of an ear. In one embodiment, the system includes an earpiece mountable within an ear canal. The earpiece includes a fluid delivery path for fluid to be delivered to the ear and a fluid removal path for fluid to be removed from the ear. The system also includes an electronics housing. The electronics housing may be directly mounted on the earpiece or positioned outside the ear. The system further includes an electrochemical gas generating device positioned within the electronics housing. In use, oxygen or the like is generated by the electrochemical gas generating device and is conveyed through the fluid delivery path of the earpiece, emerging from the earpiece distal end. The gas released from the earpiece causes fluid in the ear to be swept into the fluid removal path of the earpiece and eventually expelled to the outside of the ear.

An anatomical probe system includes an elongated flexible body including a channel defined by a wall, an operational component, a support member, an image obstruction detector, and a fluid director. The support member comprises a curved wall having a portion sized to fit within the channel and a frame shaped to retain the operational component. A frame wall is coupled to the curved wall such that the frame wall and the portion of the curved wall form an enclosed interior channel. The frame wall overlaps the portion of the curved wall in an axial direction such that a plane transverse to the axis intersects both the frame wall and the portion of the curved wall. The image obstruction detector is configured to detect an obstruction of the operational component and initiate a cleaning routine. The fluid director is configured to direct the fluid toward the operational component.