A conception device includes a dome having a collapsible sidewall, an annular rim, an integral dome rib, and three or more gripping flanges along the inner surface of the rim. The gripping flanges may effectively position and secure the device over the cervix for the concentration of semen on the cervical os to effect fertilization independently or with the aid of biologically active agents. The device may additionally include a handle extending from the annular rim at an angle.

Provided is a fertility device configured to be placed into a subject's vagina after intercourse, the fertility device comprising: a vaginal portion, the vaginal portion comprising: a proximal end; a distal end opposite the proximal end along a longitudinal axis; and a middle portion between the proximal and the distal end; and a lead operatively coupled to the proximal end, wherein: when at least part of the middle portion is placed into a subject's vagina, the lead remains partially outside the vagina, and the vaginal portion impedes leakage of sperm.

Provided is a fertility device configured to be placed into a subject's vagina after intercourse, the fertility device comprising: a vaginal portion, the vaginal portion comprising: a proximal end; a distal end opposite the proximal end along a longitudinal axis; and a middle portion between the proximal and the distal end; and a lead operatively coupled to the proximal end, wherein: when at least part of the middle portion is placed into a subject's vagina, the lead remains partially outside the vagina, and the vaginal portion impedes leakage of sperm.

The present invention relates to improved assisted reproductive technology using highly purified menotropin (HP-hMG) to stimulate follicle development in controlled ovarian stimulation, particularly in women at risk of a high ovarian response to controlled ovarian stimulation.

Everting balloon systems and methods for using the same with an alignment element for stability and anti-rotation of the everting balloon are disclosed herein. The systems can be configured to access and deliver instruments, media, or other catheters into bodily lumens and cavities. The alignment element can eliminate the potential for the everting membrane to become twisted or rotated which could impact access or the ability of the system to deliver materials. A compliance member can facilitate internal pressurization of the everting catheter system. An everting catheter system can be configured for use with transvaginal ultrasound and a lower profile speculum is described.

Everting balloon systems and methods for using the same with an alignment element for stability and anti-rotation of the everting balloon are disclosed herein. The systems can be configured to access and deliver instruments, media, or other catheters into bodily lumens and cavities. The alignment element can eliminate the potential for the everting membrane to become twisted or rotated which could impact access or the ability of the system to deliver materials. A compliance member can facilitate internal pressurization of the everting catheter system. An everting catheter system can be configured for use with transvaginal ultrasound and a lower profile speculum is described.

An oocyte retrieval needle is provided. The needle comprises a first tubular region in fluid communication with a second tubular region. The first tubular region comprises a sharp point leading end configured for insertion into a subject. The second tubular region comprises an open trailing end. The leading and trailing ends form respective opposite ends of the needle. Internal passages of the first and second tubular regions form a continuous open passage extending from the leading end to the trailing end. The first tubular region has an outer diameter which is less than an outer diameter of the second tubular region and the internal passage of the first tubular region has an inner, luminal diameter which is less than an inner diameter of the internal passage of the second tubular region. The oocyte retrieval needle is a double lumen needle.

A reproductive protection device, method and system described herein enables a user to more accurately and securely implement reproductive protection by utilizing a physical area network.

The present invention relates to improved assisted reproductive technology using highly purified menotropin (HP-hMG) to stimulate follicle development in controlled ovarian stimulation, particularly in women at risk of a high ovarian response to controlled ovarian stimulation.

The present invention relates to improved assisted reproductive technology using highly purified menotropin (HP-hMG) to stimulate follicle development in controlled ovarian stimulation, particularly in women at risk of a high ovarian response to controlled ovarian stimulation.