Viruses around the uterine orifice and in the vagina are reliably and safely removed with a simple configuration. A virus removal device includes a drive source that generates power, a contact part that comes into contact with an affected part around the uterine orifice or in the vagina, a power transmission part that transmits the power generated by the drive source to the contact part, and an operation part that operates a position of the contact part, in which the contact part is operated by the operation part while being driven by the drive source, thereby scraping tissue of the affected part. The contact part scrapes the tissue of the affected part in squamo-columnar junction, which is a common site of cervical cancer, thereby physically removing the virus contained in the tissue of the affected part to prevent and treat cervical cancer.

Viruses around the uterine orifice and in the vagina are reliably and safely removed with a simple configuration. A virus removal device includes a drive source that generates power, a contact part that comes into contact with an affected part around the uterine orifice or in the vagina, a power transmission part that transmits the power generated by the drive source to the contact part, and an operation part that operates a position of the contact part, in which the contact part is operated by the operation part while being driven by the drive source, thereby scraping tissue of the affected part. The contact part scrapes the tissue of the affected part in squamo-columnar junction, which is a common site of cervical cancer, thereby physically removing the virus contained in the tissue of the affected part to prevent and treat cervical cancer.

Systems, instruments, and methods for minimally invasive procedures including one or more of fractional resection, fractional lipectomy, fractional skin grafting, and/or fractional scar revision are described. Embodiments include instrumentation comprising a scalpet assembly coupled to a carrier, and the scalpet assembly includes a scalpet array. The scalpet array includes one or more scalpets configured for fractional resection, fractional lipectomy, fractional skin grafting, and/or fractional scar revision. The system includes a vacuum component coupled to the scalpet assembly and configured to evacuate tissue from the a site. The carrier is configured to control application of a rotational force and/or a vacuum force to the scalpet assembly.

A gynecological device that corrects a vaginal opening that is large or stretched out without requiring surgery. The stretchable gynecological device includes a main body having a front surface, a rear surface, a first end, a second end, a first edge, a second edge, and an adhesive on the rear surface of the main body. The gynecological device also includes at least two arms having a front surface, a rear surface, a first end, a second end, a first edge and a second edge that extend outwardly from the second edge of the main body. An adhesive is on the rear surface of the arms. To apply the gynecological device, the arms are firmly pressed down to the vaginal vestibule bilaterally, the main body is then pulled up above the clitoral hood and then applied and pressed down across the lower abdomen towards the anterior superior iliac spines.

A gynecological device that corrects a vaginal opening that is large or stretched out without requiring surgery. The stretchable gynecological device includes a main body having a front surface, a rear surface, a first end, a second end, a first edge, a second edge, and an adhesive on the rear surface of the main body. The gynecological device also includes at least two arms having a front surface, a rear surface, a first end, a second end, a first edge and a second edge that extend outwardly from the second edge of the main body. An adhesive is on the rear surface of the arms. To apply the gynecological device, the arms are firmly pressed down to the vaginal vestibule bilaterally, the main body is then pulled up above the clitoral hood and then applied and pressed down across the lower abdomen towards the anterior superior iliac spines.

An insertable device is designed to control uterine hemorrhaging after birth by facilitating contractile movement of the uterus. An insertable device comprises a tube having a connecting portion and a suction portion and a seal positioned along the length of the connecting portion proximal to the suction portion. Upon insertion of the suction portion and seal into the uterus, the seal abuts a vaginal canal and forms a seal between a vaginal opening and the uterus. The suction portion comprises a first loop having an opening that is oriented away from an interior wall of the uterus when inserted into the uterus. The connecting portion of the tube couples to a pump that when actuated generates a negative pressure within the uterus, resulting in a uniform mechanical stimulus to the uterine wall in order to facilitate tamponade and contractile movement of the tissue.

An insertable device is designed to control uterine hemorrhaging after birth by facilitating contractile movement of the uterus. An insertable device comprises a tube having a connecting portion and a suction portion and a seal positioned along the length of the connecting portion proximal to the suction portion. Upon insertion of the suction portion and seal into the uterus, the seal abuts a vaginal canal and forms a seal between a vaginal opening and the uterus. The suction portion comprises a first loop having an opening that is oriented away from an interior wall of the uterus when inserted into the uterus. The connecting portion of the tube couples to a pump that when actuated generates a negative pressure within the uterus, resulting in a uniform mechanical stimulus to the uterine wall in order to facilitate tamponade and contractile movement of the tissue.

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 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.

An exemplary apparatus, according to an exemplary embodiment of the present disclosure, can include, for example, a uterine manipulator having a clamp arrangement having a first tip(s) and a second tip(s), and a colpotomy ring arrangement coupled to the clamp arrangement on or at the first tip(s), and including an opening(s) in an outer surface thereof for insertion of the second tip(s) therethrough when the clamp arrangement is in a closed position. In some exemplary embodiments of the present disclosure, the clamp arrangement can include a uterine manipulator. The first tip(s) can include a plurality of removable tips, where each of the tips can have a different length from one another. In certain exemplary embodiments of the present disclosure, the first tip(s) can have a variable length.