The present invention relates to a device for treatment of erectile dysfunction comprising a ring. The device further provides for retraction of the foreskin of the user and maintains the retraction of the foreskin throughout sexual activity. Such a device also increases the length of the sliding interface of the penis during sexual activity. Further, the device will stimulate the stretch-sensitive nerve endings of the foreskin before and during sexual activity. Further, the device will increase stimulation of the sensitive nerve endings of the glans during sexual activity. The device will also retain blood within the penis upon erection, allowing for more reliable, harder and longer erection periods. The device also creates the appearance of a larger penis.

The present invention relates to a device for treatment of erectile dysfunction comprising a ring. The device further provides for retraction of the foreskin of the user and maintains the retraction of the foreskin throughout sexual activity. Such a device also increases the length of the sliding interface of the penis during sexual activity. Further, the device will stimulate the stretch-sensitive nerve endings of the foreskin before and during sexual activity. Further, the device will increase stimulation of the sensitive nerve endings of the glans during sexual activity. The device will also retain blood within the penis upon erection, allowing for more reliable, harder and longer erection periods. The device also creates the appearance of a larger penis.

This disclosure includes a system for providing sexual stimulation to a male user. The system can include a balloon having a first inner side and a second inner side located opposite the first inner side. The system can also include a tube comprising a first end and a second end located opposite the first end. The first end can be coupled to the first inner side of the balloon and the second end can be coupled to the second inner side of the balloon. When the balloon is inflated, the first end of the tube can be arranged and configured to receive an erect penis of the male user.

The present disclosure relates to a vacuum chamber extension device for penis enlargement as well as the method of assembling and using the vacuum chamber extension device for penis enlargement. The vacuum chamber extension device includes an elastic polymer sleeve configured to be positioned on the penis shaft, a glans cap configured to be placed over the glans, and a vacuum chamber configured to at least partially enclose the glans cap. The vacuum chamber extension device is safe, easy to use, effective and efficient in use. The vacuum chamber extension device can be easily secured over the penis for the purpose of penis enlargement.

The present disclosure relates to a vacuum chamber extension device for penis enlargement as well as the method of assembling and using the vacuum chamber extension device for penis enlargement. The vacuum chamber extension device includes an elastic polymer sleeve configured to be positioned on the penis shaft, a glans cap configured to be placed over the glans, and a vacuum chamber configured to at least partially enclose the glans cap. The vacuum chamber extension device is safe, easy to use, effective and efficient in use. The vacuum chamber extension device can be easily secured over the penis for the purpose of penis enlargement.

An implantable electroacupuncture device (IEAD) treats an erectile dysfunction condition of a patient through application of stimulation pulses applied at a target tissue location underlying, or in the vicinity of, at least one of acupoints BL52, BL23 or GV4. The IEAD includes an IEAD housing having an electrode configuration thereon that includes at least two electrodes, and pulse generation circuitry located within the IEAD housing and electrically coupled to the at least two electrodes. The pulse generation circuitry is adapted to deliver EA stimulation pulses to the patient's body tissue at or near the target tissue location in accordance with a specified stimulation regimen, the stimulation regimen requiring that the stimulation session have a duration of T3 minutes and a rate of occurrence of once every T4 minutes, and wherein a ratio of T3/T4 is no greater than 0.05.

An implantable electroacupuncture device (IEAD) treats an erectile dysfunction condition of a patient through application of stimulation pulses applied at a target tissue location underlying, or in the vicinity of, at least one of acupoints BL52, BL23 or GV4. The IEAD includes an IEAD housing having an electrode configuration thereon that includes at least two electrodes, and pulse generation circuitry located within the IEAD housing and electrically coupled to the at least two electrodes. The pulse generation circuitry is adapted to deliver EA stimulation pulses to the patient's body tissue at or near the target tissue location in accordance with a specified stimulation regimen, the stimulation regimen requiring that the stimulation session have a duration of T3 minutes and a rate of occurrence of once every T4 minutes, and wherein a ratio of T3/T4 is no greater than 0.05.

A system and method directed for a sizing device and erectile ring is described where the sizing device properly measures one's girth to correctly find the proper size erection ring. The sizing device has a measuring tape that will slide through a plurality of perimeter components with a track running through each of the perimeter components for the measuring tape to easily travel through whereby a measurement is then obtained when the perimeter components come into contact with the penis whereby then an erectile is created from the sizing.

A system and method directed for a sizing device and erectile ring is described where the sizing device properly measures one's girth to correctly find the proper size erection ring. The sizing device has a measuring tape that will slide through a plurality of perimeter components with a track running through each of the perimeter components for the measuring tape to easily travel through whereby a measurement is then obtained when the perimeter components come into contact with the penis whereby then an erectile is created from the sizing.

An at least partly implantable system for injecting a substance into a patient's body, in particular a penis erection stimulation system, comprises one or more infusion needles disposed within and implanted along with one or more housings adjacent the patient's left and right corpora cavernosa. A reservoir and a pump are also implanted inside the patient's body to supply the infusion needle with infusion liquid. A drive unit also adapted for implantation inside the patient's body is arranged for advancing and retracting the tip end of the infusion needle such that it penetrates the housing at least in two different penetration areas either simultaneously or in immediate time succession, thereby injecting drugs along with the infusion liquid into the patient's body for stimulating penis erection. The drive unit is configured to laterally displace the tip end of at least one infusion needle in at least two different lateral directions to different penetration sites within said at least one penetration area.