The present invention relates to an ultrasonic probe injection device using RCM, the device enabling the insertion angle and the insertion depth of an injection needle of an injection unit to be easily adjusted using one hand, and the insertion angle and the insertion depth of the injection needle of the injection unit to be automatically fixed after adjustment, thereby having the merit of enhancing efficiency in operation, and even if the insertion angle of the injection needle of the injection unit changes, the insertion point reached when the injection needle of the injection unit is inserted is equally maintained, thereby having the merit of enabling a decrease in error with respect to a lesion area.

A medical power supply system includes: a medical device including an elongated insertion section, a power receiving unit including a power receiving member and movable relative to the insertion section in a longitudinal direction of the insertion section, and a biasing unit biasing the power receiving unit toward a distal end side of the insertion section; and a guide unit including a power transmitting unit including a power transmitting member, the insertion section being inserted into the guide unit. When the insertion section is inserted into the guide unit to a predetermined amount, the power receiving unit comes in contact with the power transmitting unit with being biased by the biasing unit, and the power transmitting member and the power receiving member face each other in an axial direction of the insertion section and have a positional relation in which wireless power transmission is possible.

A system for treatment of obstructive sleep apnea (OSA) is described. The system includes an introducer needle having an elongated body. The introducer needle is configured to create an opening in a tongue of a patient for implantation of a lead for treating OSA. One or more electrically conductive areas are located on the elongated body. A medical device is configured to deliver a stimulation signal via the introducer needle through the one or more electrically conductive areas to the tongue of the patient to stimulate one or more motor points of a protrusor muscle within the tongue of the patient.

The present invention presents an apparatus and methods to guide insertion of invasive devices to a tissue target of a living body. The apparatus comprises a positioning guide control assembly and a positioning guide assembly that is operably detachable from the control assembly, and rotationally adjustable and lockable. The positioning guide control assembly releasably houses a ultrasound transducer head and measures an insertion length and an insertion angle of an invasive device placed in the positioning guide assembly to reach the tissue target.

A biopsy device includes a lateral member; a gun mount configured to support a biopsy gun, the gun mount being connected to the lateral member and movable along a first axis with respect to the lateral member, and a sensor which detects a position of the gun mount along the first axis with respect to the lateral member and generates positional data which is provided to an interface module. The gun mount can also be reconfigured in orientations which are offset in a dimension which is orthogonal to the first axis, orientations rotationally offset about the first axis or an axis parallel to the first axis. The lateral member can be in right hand and left hand orientations. Various sensors detect these reconfigurations and provide corresponding data to the interface module for additional calculations and display.

Practitioners who use sacral neuromodulation on a regular basis have sought ways to simplify the procedure and performing percutaneous nerve evaluations in the office setting have become increasingly more popular. However, many practitioners are limited by the lack of availability of fluoroscopy or similar imaging systems in the office setting and do not feel comfortable executing the procedure without it, for a variety of reasons. The disclosed system and method demonstrate an avenue to circumvent the lack of fluoroscopic guidance in the office setting enabling execution of percutaneous nerve evaluations successfully and efficiently.

A cover for magnetizing a shaft of a tissue-penetrating medical device is disclosed including a sleeve member having a hollow body to form a protective closure over the shaft of the tissue-penetrating medical device. The open end of the hollow body provides a receiving space for receiving the shaft of the tissue-penetrating medical device. A magnet is disposed on the sleeve member. Medical devices and methods of magnetizing the shaft of a tissue-penetrating medical device using the cover are also disclosed.

A medical device such as a needle subassembly is disclosed including a cover over a magnetized portion of a tissue-penetrating medical device having a shielding material associated with the cover that prevents the magnetized portion of the tissue-penetrating medical device from being de-magnetized when the cover is positioned to cover the tissue-penetrating medical device.

An intervention system employs an optical shape sensing tool (32) (e.g., a brachytherapy needle having embedded optical fiber(s)) and a grid (50, 90) for guiding an insertion of the optical shape sensing tool (32) into an anatomical region relative to a grid coordinate system. The intervention system further employs a registration controller (74) for reconstructing a segment or an entirety of a shape of the optical shape sensing tool (32) relative to a needle coordinate system, and for registering the needle coordinate system to the grid coordinate system as a function of a reconstructed segment/entire shape of the optical shape sensing tool (32) relative to the grid (50, 90) (i.e., reconstruction of a segment/entire shape of the OSS needle inserted into/through the grid serving as a basis for the grid/needle coordinate system registration).

The present disclosure is directed to devices, kits, and methods for treating lumbar spinal stenosis by at least partially decompressing a compressed nerve root. The method can include identifying the compressed nerve root and percutaneously accessing a region of a lamina located adjacent to the compressed nerve root. The method can also include forming a channel through the region of the lamina, wherein the channel can be formed medial to a lateral border of the lamina. Further, the method can include expanding the channel in a lateral direction.