A surgical needle is configured to detect whether a distal tip of the surgical needle perforates or ends up in an undesirable location, or detect whether the distal tip of the surgical needle has accessed a desired location. The surgical needle includes a hub and a body connected to the hub. The body has a hollow core and includes a sharp-pointed tip at a distal end. A first electrode is formed by the sharp-pointed tip of the body. At least a second electrode is provided around the body. The first and second electrodes are connected to a wired connector that can be plugged into an external sensing system. The external sensing system can monitor impedance, electrical parameters, or other parameters.

Systems and methods for treating an aneurysm in accordance with embodiments of the present technology include intravascularly delivering an occlusive member to an aneurysm cavity and deforming a shape of the occlusive member via introduction of an embolic element to a space between the occlusive member and an inner surface of the aneurysm wall.

A compact ultrasonic transducer for an ultrasonic surgical instrument includes a proximal casing defining a hollow interior and a piezoelectric rod array including a plurality of piezoelectric rods radially spaced-apart from one another and arranged in a longitudinally-oriented direction. The piezoelectric rod array is disposed within the hollow interior. The compact ultrasonic transducer further includes a distal horn including a distal connector configured to engage a waveguide. The distal horn is configured to engage the proximal casing to enclose the piezoelectric rod array within the hollow interior. An ultrasonic surgical instrument including the compact ultrasonic transducer is also provided.

A surgical system includes a surgical instrument having a body, a shaft extending distally from the body, an ultrasonic transducer supported by the body, and an end effector at a distal end of the shaft. The end effector includes an ultrasonic blade configured to be driven by the ultrasonic transducer with ultrasonic energy, and an RF electrode operable to seal tissue with RF energy. A generator is operatively coupled with the surgical instrument and is operable to generate a combined drive signal having an ultrasonic energy component and an RF energy component. Filter circuitry arranged externally of the body of the surgical instrument is operable to convert the combined drive signal to an ultrasonic drive signal configured to energize the ultrasonic transducer to drive the ultrasonic blade with ultrasonic energy, and an RF drive signal configured to energize the RF electrode with RF energy sufficient to seal tissue.

A tissue displacement/separation device includes a seamless bladder constructed of a biodegradable polymer. The bladder is expandable from a collapsed or rolled state for insertion into a body between a first and second tissue to an expanded state for separating the first and second tissue.

A collapsible detection antenna (10) to detect electromagnetic tags (12) of surgical articles (14) in an operating room (16) includes an antenna assembly (18) configured to detect the electromagnetic tags (12). The antenna assembly (18) is configured to move between a deployed configuration and a collapsed configuration. In the deployed configuration, the antenna assembly forms an antenna loop (20) configured to detect the electromagnetic tags (12). The antenna assembly (18) has a greater detection range in the deployed configuration than in the collapsed configuration. The deployed configuration corresponds to a tuned shape of the antenna assembly (18) sufficient to detect the electromagnetic tags (12) in the deployed configuration.

A retractor member is configured for insertion through a channel of an access member and for moving soft tissue at a treatment site that is accessible through the channel. The retractor includes a body having a proximal end and a distal end and spaced from each other along a longitudinal direction. The distal end defines a retractor blade and the body defines a first surface and a second surface opposite each other along a transverse direction substantially perpendicular to the longitudinal direction. The retractor includes an attachment device configured to selectively attach the body to a portion of the access member such that the body is extendable through the working channel while the body is attached to the portion of the access member.

Retrieval of material from vessel lumens can be improved by electrically enhancing attachment of the material to the thrombectomy system. The system can include a catheter having a distal portion configured to be positioned adjacent to a thrombus in a blood vessel, an electrode disposed at the distal portion of the catheter, and an interventional element configured to be delivered through a lumen of the catheter. The electrode and the interventional element are each configured to be electrically coupled to an extracorporeal power supply.

A dual-motion rotation and retraction system for forming a pathway to a patient's intervertebral disc space includes a dilator, retractable dual-blade assembly, and dual-motion retractor. The dilator may feature a narrow rectangular, elliptical, or elongated configuration body for insertion parallel to the fibers of the psoas muscle, including an angle of 0 to 90 degrees to the patient's spine. The dual-blade assembly includes opposing blade subassemblies, each having a blade bordered by adjustable wings, along with built-in lighting and video capabilities. The dual-blade assembly may be passed over the dilator at the insertion orientation. The dual-motion retractor may be disposed about the dual-blade assembly and dilator and employed to both rotate the dual-blade assembly and the dilator 0 to 90 degrees to a final rotated orientation parallel to the intervertebral disc space and to retract the opposing blade subassemblies away from one another to create the surgical pathway. Other embodiments are also disclosed.

An occlusive implant for bifurcation aneurysms (A), with the implant (1) being in an expanded state in which it is implanted in the blood vessel and in a contracted state in which it is movable through the blood vessel, with the implant (1) having a proximal fixing section (3) by means of which the implant (1) can be secured to the wall of a blood vessel, a distal section (5) where the implant (1) in expanded state is radially widened relative to the fixing section (3) and which is intended for placement in or in front of the aneurysm (A), and having a transition section (4) located between the fixing section (3) and the distal section (5), wherein fixing section (3) is attached to an delivery wire (2) in a detachable manner and wherein the transition section (4) has a second detachment point (7) which enables the distal section (5) to be detached.