A surgical handpiece for removing tissue includes a housing defining a cavity therein, the housing having a proximal hub connector disposed at a distal end thereof. An end effector assembly is operably supported by the proximal hub connector and includes an outer shaft supporting a cutting shaft configured to remove tissue upon activation thereof via translation or rotation. A fluid pump is disposed within the cavity of the housing and is configured to evacuate fluid from the cutting shaft upon activation thereof. A motor is disposed within the cavity of the housing and includes a power coupler operably coupled to both the cutting shaft and the fluid pump for suppling power thereto.

A colposcopy instrument (which includes a display screen) is controlled by a specific set of steps defined in software to follow a defined protocol for performing a colposcopy examination. The software is utilized to also control the features of an included camera so that consistent digital images are recorded. The integrated software prompts the medical personnel performing the colposcopy procedure to capture relevant images in an automated sequence that includes, for example, capturing a sequence of images after the application of the acetic acid to the cervix. The displayed user interface guides the individual performing the exam through a series of easy-to-understand screen prompts to capture specific, critical images during the exam. The process, once begun, is automated and does not require the individual performing the exam to make any decisions about whether or not to record a certain image.

A colposcopy instrument (which includes a display screen) is controlled by a specific set of steps defined in software to follow a defined protocol for performing a colposcopy examination. The software is utilized to also control the features of an included camera so that consistent digital images are recorded. The integrated software prompts the medical personnel performing the colposcopy procedure to capture relevant images in an automated sequence that includes, for example, capturing a sequence of images after the application of the acetic acid to the cervix. The displayed user interface guides the individual performing the exam through a series of easy-to-understand screen prompts to capture specific, critical images during the exam. The process, once begun, is automated and does not require the individual performing the exam to make any decisions about whether or not to record a certain image.

The present disclosure is directed to arthroscopic visualization systems and methods. The visualization system can include a camera with a fluid inflow path, wherein a proximal end of the camera is configured to fluidly connect a fluid reservoir to the fluid inflow path. The system can also include a cannula with a lumen, wherein the lumen is configured to be fluidly connected to the fluid inflow path at a distal end of the camera. In addition, the system can also include a scope, wherein the scope is configured to be connected to the distal end of the camera and a portion of the scope is configured to be inserted into the lumen of the cannula.

Medical devices and methods related to endoscopic systems suitable for hysterectomy and other purposes.

Medical devices and methods related to endoscopic systems suitable for hysterectomy and other purposes.

Systems and methods are provided for treating cervical and/or uterine cancers in brachytherapy with an intracavitary brachytherapy applicator. The system comprises a tandem adapted for insertion into a cervix of a patient. An ovoid assembly comprises first and second inflatable ovoids and an ovoid support mechanism. The first and second inflatable ovoids are adapted for insertion within fornices of a patient. First and second retractors are adapted to be coupled to the ovoid assembly. The first retractor is adapted to be positioned to retract the bladder of a patient during treatment. The second retractor is adapted to be positioned to retract the rectum of a patient during treatment. The tandem and the first and second inflatable ovoids are adapted to be coupled to a radioactive source to deliver a radiation dose suitable for cancer treatment at a cancerous cervical treatment site in a patient.

Systems and methods are provided for treating cervical and/or uterine cancers in brachytherapy with an intracavitary brachytherapy applicator. The system comprises a tandem adapted for insertion into a cervix of a patient. An ovoid assembly comprises first and second inflatable ovoids and an ovoid support mechanism. The first and second inflatable ovoids are adapted for insertion within fornices of a patient. First and second retractors are adapted to be coupled to the ovoid assembly. The first retractor is adapted to be positioned to retract the bladder of a patient during treatment. The second retractor is adapted to be positioned to retract the rectum of a patient during treatment. The tandem and the first and second inflatable ovoids are adapted to be coupled to a radioactive source to deliver a radiation dose suitable for cancer treatment at a cancerous cervical treatment site in a patient.

A device for visualization of internal tissue of a patient's uterus, the device including a hand-held control unit, an elongated member, and an image capturing tip. To provide better light conditions, to reduce heat generation and related problems with excessive heating and to improve the ergonomic conditions, a device including an illumination structure having at least a first and a second optical fibre is provided.

A device for visualization of internal tissue of a patient's uterus, the device including a hand-held control unit, an elongated member, and an image capturing tip. To provide better light conditions, to reduce heat generation and related problems with excessive heating and to improve the ergonomic conditions, a device including an illumination structure having at least a first and a second optical fibre is provided.