Disclosed is a surgical instrument comprising an end effector with energy sensitive resistance elements.

A retractor blade includes a descender portion and a hook portion. The descender portion is configured to engage a rib in response to a retraction force applied to the retractor blade. The hook portion forms a channel with the descender portion. The channel is configured to secure the rib against the descender portion. The descender portion and the hook portion are integrally formed of a compliant material. The first hook portion includes at least one gap separating a plurality of teeth. The at least one gap of the hook portion and the compliant material together are configured to cause substantially an entire length of the retractor blade in the descender portion to conform to the rib in response to the retraction force. The retractor blade may be pivotably attached to an arm of a retractor that is configured to mechanically retract in response to the retraction force.

Exclusion devices for anatomical structures, and related instruments and related methods, are disclosed. An exclusion device for an anatomical structure may include a first beam, a second beam, and/or a first spring operatively coupled to the first beam and the second beam to exert a closing force on the first beam and the second beam. The first spring may be generally U-shaped and/or may include a first end portion and a second end portion generally opposite a connecting portion.

A method for deforming a staple comprising a base, a first staple leg, and a second staple leg, wherein the base, the first staple leg, and the second staple leg are positioned within a common plane prior to being deformed, the method comprising positioning the first staple leg within a first cup of a staple pocket, the first cup comprising a first inner surface, applying a first compressive force to the first staple leg to bend the first staple leg toward the base and the second staple leg, contacting the first inner surface with the end of the first staple leg to bend the end of the first staple leg toward a first side of the base, and deforming the first staple leg such that the end of the first staple leg crosses a mid-line of the staple defined between the first staple leg and the second staple leg.

An all-suture anchor for generating bone compression and increasing interference fixation. The all-suture anchor includes a fibrous construct which is movable between a pre-deployment configuration and a deployed configuration. The fibrous construct has a first density. The all-suture anchor also includes a monofilament woven through the fibrous construct. The monofilament has a second density, which is different than the first density. The contrasting densities (i.e., irregularities) aids in the “locking” ability of the all-suture anchor by greater purchase in hard and soft bone. The all-suture anchor can have a variety of textures, barbs, and rigidities that aid in creating irregularities within the bone surface for more secure fixation.

A reusable surgical device includes a housing or body that supports one or more thermal energy storage members that retain or store heat during a cleaning and sterilization process. The stored heat functions to evaporate water that remains within the body or housing of the surgical device after the cleaning and sterilization process is completed to minimize any likelihood of infection of a patient or damage to electronics within the surgical device that may result or occur due to the presence of the water within the surgical device.

A trans-anastomotic insertion device includes a body having a distal portion, a proximal portion, and a central portion. The distal portion has a blunt distal end, a width that decreases from its distal end to its proximal end, and longitudinal ribs that provide rigidity to the distal portion. The central portion has a circular configuration and includes a proximally facing surface that includes protrusions that are positioned to be received within staple pockets of a reload assembly of a stapling device. The proximal portion includes a central post that includes splines that are received between splines on a shell housing of a stapling device. The configuration of the insertion device provides added strength to the insertion device to resist high torsional forces that may be applied to the insertion device during insertion of a surgical device through an incision into a body cavity.

An apparatus (20) includes a tube (22), configured to advance to a blockage, and including a proximal hub (24) configured to connect to a suction-applying device such that, following the advancement of the tube to the blockage, a suction force generated by the suction-applying device is applied, via the tube, to the blockage, a shaft (26), including first and second electrically-conductive circumferential portions (28, 30), configured to pass through the tube, and first and second electrically-conductive elements (34, 38), configured to connect the first and second electrically-conductive circumferential portions to respective terminals of a power source (36). The first electrically-conductive circumferential portion is configured to attract the blockage when a voltage is applied by the power source, via the first and second electrically-conductive elements, between the first and second electrically-conductive circumferential portions, such that the blockage is anchored to the shaft while the suction force is applied to the blockage.

A medical device for performing a hysterectomy is provided. The medical device has a tissue incision assembly that includes a first cup nested within a second cup. The tissue incision assembly also includes a spacer assembly between the first cup and the second cup in order to maintain a spacing between the first and second cups. The tissue incision assembly also has a cutting implement that has a portion extending between, and movable with respect to, the first and second cups. The cutting implement can provide a circular cut guided via the spacing between the first and second cups.

A circular stapling device for performing anastomosis procedures includes an end effector that includes or is adapted to deliver probiotics to an anastomotic site during formation of the anastomosis.