Patent application number | Description | Published |
20090171143 | DEVICES AND METHOD FOR TREATING PELVIC DYSFUNCTIONS - In one embodiment, a method includes securing an implant that includes a pre-formed loop to a vaginal apex. An end of the suture is inserted through a selected portion of a pelvic tissue to dispose at least a portion of the implant within a pelvic region of the patient. The end of the suture is drawn through the loop while simultaneously advancing a uterus to approximate the vaginal apex to the selected portion of pelvic tissue. An apparatus includes an implant and a suture coupled to the implant having a pre-formed loop. configured to receive a portion of a delivery device therethrough. A trocar is coupled to an end of the suture that can be releasably coupled to an end of the delivery device. The trocar can be inserted through a pelvic tissue and drawn through the loop forming a knot to secure the implant to the pelvic tissue. | 07-02-2009 |
20100081866 | Pelvic Floor Mesh and Incontinence Sling - A support device includes a support member and a frame member. The support member has a body portion and an elongated arm extending from the body portion. The elongated arm has a width smaller than a width of the body portion of the support member. The body portion is configured to help support an anatomical structure located in a pelvic region of a patient. The frame member is coupled to the support member and comprised of a shape memory alloy. | 04-01-2010 |
20100312043 | SYNTHETIC GRAFT FOR SOFT TISSUE REPAIR - An implant includes a support member having a first portion and a second portion. The support member is configured to be in contact with a wall of a vagina of a patient. The first portion defines apertures having a first size. The second portion defines at least one aperture having a second size. The second size is larger than the first size. The aperture having the second size is configured to be substantially aligned with a scar or an incision in the wall of the vagina. The second portion is configured to better prevent erosion of the wall of the vagina near the scar or incision than the first portion. | 12-09-2010 |
20110106108 | DEVICE AND METHOD FOR DELIVERY OF MESH-BASED DEVICES - In some embodiments, a stylet includes a proximal end portion, a distal end portion, and a medial portion between the proximal end portion and the distal end portion. The distal end portion of the stylet is configured to be releasably coupled to a first portion of an implant. The medial portion of the stylet has at least one retention member configured to be releasably coupled to a second portion of the implant. | 05-05-2011 |
20110152914 | LESS TRAUMATIC METHOD OF DELIVERY OF MESH-BASED DEVICES INTO HUMAN BODY - In some embodiments, a method includes extending a dilator into a body of a patient in a first direction such that a distal end portion of the dilator extends from the body. The dilator defines a lumen therethrough. At least a portion of the dilator is disposed within the body when the distal end portion extends from the body. At least a portion of an implant is passed through the lumen defined by the dilator. The dilator is removed from the body by moving the dilator in the first direction. | 06-23-2011 |
20110184228 | COMPOSITE SURGICAL IMPLANTS FOR SOFT TISSUE REPAIR - According to one aspect of the invention, composite implants for soft tissue repair a provided which comprise (a) a substantially two-dimensional piece of biologic matrix material and (b) one or more non-absorbable synthetic polymeric filaments. | 07-28-2011 |
20120029274 | IMPLANTS AND METHODS OF IMPLANTING THE SAME - In one embodiment, an apparatus includes a support member and a suture. The support member is configured to provide support to a portion of a body of a patient. The support member has a first end portion and a second end portion. The first end portion of the support member is configured to be disposed within a body of a patient. The suture is removably coupled to the first end portion of the support member and is configured to extend through an incision in the body of the patient from a location within the body of the patient to a location outside of the body of the patient. | 02-02-2012 |
20120059217 | PELVIC IMPLANTS AND METHODS OF IMPLANTING THE SAME - In one embodiment, an implant is configured to be placed within a body of a patient. The implant includes a support member. The support member is configured to be placed adjacent a vaginal apex of a patient. The support member has a length sufficient to extend the length of the vaginal apex but not of a length sufficient to extend from the vaginal apex to a location between a vagina of the patient and a rectum of the patient. The implant also includes first and second arm members coupled to the support member. The arm members are configured to be coupled to bodily tissue of the patient to help secure the implant within the body of the patient. | 03-08-2012 |
20120289980 | ANCHORS FOR BODILY IMPLANTS AND METHODS FOR ANCHORING BODILY IMPLANTS INTO A PATIENT'S BODY - An anchor is provided for anchoring a bodily implant within a body of a patient. The anchor includes an implant engaging portion for engaging the bodily implant, wherein the implant engaging portion is disposed on a lateral portion of the anchor. The anchor further includes a distal end portion configured to pass through a passageway in the patient's body, the passageway defining a first axis and a proximal end portion disposed longitudinally opposite to the distal end portion on the anchor. The anchor defines a second axis extending from the distal end portion to the proximal end portion. The anchor is configured to rotate when a force is applied to the bodily implant such that the second axis defined by the anchor forms an angle with the first axis defined by the passageway. | 11-15-2012 |
20130041398 | Dilator - A device for dilating a body passage includes an inner element including a shaft portion extending longitudinally from a proximal end to a distal end and an enlarged portion situated in the distal end and an outer sleeve extending longitudinally from a proximal end to a distal end and including a lumen extending therethrough. The lumen is sized and shaped to slidably accommodate the shaft portion of the inner element such that the device is movable between an insertion configuration, in which the enlarged portion extends distally past the distal end of the outer sleeve, and an expanded configuration, in which the distal end of the outer sleeve receives the enlarged portion of the inner element therein. | 02-14-2013 |
20130178696 | BODILY IMPLANTS FORMED FROM DIFFERENT MATERIALS - In one embodiment, an implant includes a body member and an extension member. The body member is formed of a first material and has a first side portion and a second side portion. The extension member is formed of a second material different than the first material. The extension member has a first arm portion, a second arm portion, and a mid-portion disposed between the first arm portion and the second arm portion. The mid-portion extends from the first side portion of the body member to the second side portion of the body member. The first arm portion extends from the first side portion of the body member along a first axis. The second arm portion extends from the second side portion of the body member along a second axis different than the first axis. | 07-11-2013 |
20140221731 | SYSTEMS AND METHODS FOR SLING DELIVERY AND PLACEMENT - The invention, in various embodiments, is directed to systems, devices, and methods relating to pre-pubic approaches to delivering a supportive sling to periurethral tissue of a patient. | 08-07-2014 |
20150057491 | MEDICAL DEVICE AND METHOD OF DELIVERING THE MEDICAL DEVICE - The invention discloses an implant. The implant may include a first flap and a second flap. The first flap may further include a first portion, a second portion and a transition region. The first portion may be configured to be attached proximate a sacrum. The second portion may be configured to be attached to an anterior vaginal wall. The transition region lies between the first portion and the second portion. The second flap may be fabricated such that a portion of the second flap is configured to be attached to a posterior vaginal wall. The implant may be configured such that a value corresponding to a biomechanical parameter defining a biomechanical attribute of the portion of the first flap attaching to the anterior wall is different from a value of the biomechanical parameter defining the biomechanical attribute of the portion of the second flap attaching to the posterior wall. | 02-26-2015 |