An example assembly for use with a vacuum system and an esophageal positioning device esophageal positioning device includes an introducer, in which the esophageal positioning device includes a first segment and a second segment. The second segment is pivotally connected to the first segment. A gap portion of an outer tube of the introducer is defined along a longitudinal axis between a tube tip of the introducer and the distal end of the second segment of the esophageal positioning device when the esophageal positioning device is disposed within the introducer. The gap portion defines one or more radial vacuum holes.

A cannula seal assembly with a compatible flexible cannula. The cannula includes a rigid cannula body having proximal and distal body ends. The cannula body is composed of material having a first thickness. A flexible thread extends along at least a portion of the cannula body from the distal body end toward the proximal body end. The thread is composed of material having a second thickness, which is less than a first thickness. The cannula is attachable to a cannula seal assembly. The assembly includes a housing having a primary seal and a secondary seal therein. The assembly has a spacer connected between the primary seal and the secondary seal and a reservoir between the primary seal and the secondary seal.

The implantable nerve blocking intervention involves performing a first subdermal incision on the ventral lateral portion of the patient's thorax. A first end of a tunneling device is inserted through the first subdermal incision. The tunneling device is traversed below the patient's dermal layer towards the mid axillary line. The tunneling device is traversed above the lower section of the rib cage towards the patient's paralumbar line. A longitudinal paramidline incision is performed about 3 inches lateral to the vertebral body and the tunneling device. A needle or trocar tip is inserted through the paramidline incision towards a primitive cluster of nerves and a catheter is placed through the needle or trocar which is removed prior to anchoring the catheter. A catheter tube is inserted through the length of the tunneling device. The catheter tube is coupled to the distal catheter. The tunneling device is retracted over the catheter tube. The catheter tube is coupled to a percutaneous access port.

A probe unit includes, a probe configured to treat a bone by ultrasonic vibration, a hollow sheath which surrounds the probe and which has a first portion at a small distance from a central axis, and a second portion at a greater distance from the central axis than the first portion, and a knob configured to rotate the sheath relative to the probe between a first position for insertion between the bone and a living tissue facing the bone so that the first portion is located between the bone and the living tissue and a second position for insertion between the bone and the living tissue so that the second portion is located between the bone and the living tissue.

Surgical access stabilization devices, systems, and methods are disclosed herein. For example, the devices, systems, and methods disclosed herein can be used during a surgical procedure to selectively establish, stabilize, and maintain a desired trajectory and/or positioning of a surgical access device. An exemplary surgical access stabilization device can include a pad with an adhesive distal facing surface to adhere to an anchor surface, a surgical access device coupled to the pad, and a locking mechanism to selectively lock a position of the surgical access device relative to the pad. In one embodiment, the anchor surface can be the skin of a patient. An exemplary surgical access device stabilization method can include making an incision in a patient at a surgical site, inserting a surgical access device through the incision, adhering a pad to an anchor surface, e.g., the skin of the patient, coupling the surgical access device to the pad, and selectively locking a position of the surgical access device relative to the pad. Other exemplary devices, systems, and methods are also provided.

Surgical visualization systems and related methods are disclosed herein, e.g., for providing visualization during surgical procedures. Systems and methods herein can be used in a wide range of surgical procedures, including spinal surgeries such as minimally-invasive fusion or discectomy procedures. Systems and methods herein can include various features for enhancing end user experience, improving clinical outcomes, or reducing the invasiveness of a surgery. Exemplary features can include access port integration, hands-free operation, active and/or passive lens cleaning, adjustable camera depth, and many others.

A cannula for use in a terminable intraosseous device comprises a cannula body, and a penetrator-independent proximal bone penetration indicator (PBPI) associated with the body for positively indicating initial penetration into the proximal bone. In various embodiments, the PBPI comprises a roughened surface provided at a distal end of the cannula body to assist in increasing an amplitude of vibrations that are generated immediately upon contact with a proximal bone cortex during performance of an intraosseous injection, a resilient element fixed at one end which becomes plastically deformed, a visually indicative element which is exposed when the distance between the cannula body and penetrator is changed, or a frictionally engageable element. In some embodiments, a stopper prevents additional penetration into the proximal bone, and a reinforcing member inserted within a cannula body lumen reinforces a thin-walled portion of the cannula body.

A method of viewing the contents of a specimen bag includes, placing tissue within a cavity of the specimen bag through an open end of the specimen bag, engaging a stretchable portion of the specimen bag with a scope to stretch the stretchable portion of the specimen bag, and operating the scope to view the contents of the specimen bag.

A threading support facility is for threading an object into a guide apparatus. The threading support facility is connectable to the guide apparatus and is configured to support threading of the object into the guide apparatus. In an embodiment, the threading support facility includes a wall connecting a first aperture of the threading support facility and a second aperture of the threading support facility. The first aperture is embodied as an inlet for insertion of the object into the threading support facility and the second aperture is embodied as an outlet out of the threading support facility. Further, a sub-guide runs along the wall of the threading support facility and runs in a direction from the first aperture to the second aperture. The sub-guide is configured to support guiding of the object, after insertion through the first aperture, into the threading support facility in a direction of the second aperture.

An integrated sheath assembly for inserting a medical device such as a percutaneous pump into a vessel can include a first sheath having a first lumen defining a first opening between proximal and distal ends of the first sheath for passage of a portion of the pump and a second sheath having a second lumen defining a second opening between proximal and distal ends of the second sheath. The second lumen is expandable to allow passage of the first sheath containing the portion of the pump. The first sheath fills a space between the second sheath and the portion of the percutaneous pump when the first sheath containing the percutaneous pump is inserted into the second lumen. The first sheath has a first hub, and the second sheath has a second hub. In some embodiments, a single sheath and a movable connector can be integrated on the medical device.