A tray for securing an implantable device to a carrier member includes a slot configured to retain the carrier member and a receptacle adjacent the slot. The carrier member surrounds a shaft of the implantable device. The receptacle has a first width at a proximal end of the receptacle to receive first and second arms of the implantable device in an initial state in which the first and second arms extend substantially perpendicularly from the shaft. The receptacle has a second width at a distal end of the receptacle for receiving the first and second arms of the implantable device in a collapsed state in which the first and second arms are folded against the shaft such that the carrier member can be slid over the first and second arms to retain the first and second arms. The second width is less than the first width.

A sexual accessory pack comprising a transparent or translucent sterile ring pack including a penile ring enclosed therein by a releasable film having a pull tab, where the ring pack is removably attached to the outer surface of a condom pack to provide integral packaging of sexual accessories. One or more sexual accessory packs are packaged in an at least partially transparent or translucent retail, such as a transparent or translucent window, to allow purchasers to visually access various characteristics of the packaged penile rings, such as style, shape and size, prior to completing a purchase.

A tray for securing an implantable device to a carrier member includes a slot configured to retain the carrier member and a receptacle adjacent the slot. The carrier member surrounds a shaft of the implantable device. The receptacle has a first width at a proximal end of the receptacle to receive first and second arms of the implantable device in an initial state in which the first and second arms extend substantially perpendicularly from the shaft. The receptacle has a second width at a distal end of the receptacle for receiving the first and second arms of the implantable device in a collapsed state in which the first and second arms are folded against the shaft such that the carrier member can be slid over the first and second arms to retain the first and second arms. The second width is less than the first width.

Delivery systems and methods for forming and delivering biomaterials from two components are described herein. In particular, apparatus and methods for performing controlled delivery of multicomponent delivery of biomaterials into or onto a body part, such as a body lumen are described. More specifically, in some embodiments, the apparatus and methods are directed towards controlled delivery of micro-volumes of biomaterials into or onto a target location, the micro-volumes being defined as 0.001 mL-1 mL (or 1 μL-1,000 μL) of volume.

A packaged condom applicator apparatus is provided with a condom supplied therein. The apparatus has the following: a condom holder where the base of the condom can be inserted and secured in place while protecting the condom body as packaging; an apparatus clip or unhinged clip that presses down on the condom tip to create a reservoir and an airtight seal during condom application. This helps avoid the creation of air bubbles. Using the condom holder, the user simply slides the condom along the erected penis to apply the condom on and removes the condom holder, opening the condom tip clip automatically, and ejecting the whole apparatus after the condom is applied onto the penis. Using this self-applicable apparatus, the user can quickly use the condom with less effort, distraction, and manual intervention.

The present invention relates to a male contraception apparatus for obtaining a time-limited sterility of a male mammalian individual. The apparatus comprises a restriction device adapted to restrict the lumen of a vas deferens of the mammalian, and a controller operable to control the restriction device to restrict the lumen of the vas deferens during a controlled period to prevent sperms from reaching the urethra of the mammalian. The apparatus further comprises an implantable constriction device configured to gently constrict at least one portion of a tissue wall of the vas deferens to restrict the lumen of the vas deferens such that the flow of sperms in the vas deferens is restricted, and a stimulation device configured to stimulate the constricted wall portion of the tissue wall.

A condom is configured to include a space such that a front glans part of the condom does not excessively come into contact with the penis of a man by selecting a material having moderate elasticity such as soft synthetic resin or synthetic latex rubber or a foamed rubber material conforming thereto or the like for the front part of the condom made from a soft rubber material; and includes embossed sponge layers or fine soft hairs additionally laminated on the inside and outside of the condom, to provide an excellent moisturizing effect such that an excellent contraceptive effect and a sexual pleasure-increasing effect can be simultaneously obtained when a user wears the condom, thereby providing multiple effects such as contributing to the treatment of patients with chronic dyspareunia or patients with anorgasmia and the like.

Delivery systems, compositions, and methods for forming and delivering biomaterials from two components are described. Specifically, a composition includes a first component and a second component that are each formulated to be crosslinked with the other to form a hydrogel. The first component and the second component are formulated to have an initial storage modulus (initial G) and an initial loss modulus (initial G″) when initially combined such that a ratio of the initial G″ to the initial G is between about 5 and about 100. The first component and the second component are formulated to have a gelation storage modulus (gelation G) and a gelation loss modulus (gelation G″) at a gelation time after the first component and the second component are combined such that a atio of the gelation G″ to the gelation G is less than about 1. The gelation time is less than about 120 seconds.

Applicator for delivering an occluding compound in a fallopian tube includes a lumen extending between a proximal end connectable to a dispenser for containing uncured occluding compound, and a distal end. A spiral wire with a first end is connected to the distal end of the lumen and a free second end. A disconnecting member is configured to disconnect the spiral wire from the distal end. An actuator is configured to actuate the disconnecting member. The distal end of the lumen can be inserted into the fallopian tube. The spiral wire functions as a guide wire. The curable compound embeds the spiral wire. The actuator can be actuated to disconnect the embedded spiral wire from the distal end of the lumen.

Delivery systems and methods for forming and delivering biomaterials from two components are described herein. In particular, apparatus and methods for performing controlled delivery of multicomponent delivery of biomaterials into or onto a body part, such as a body lumen are described. More specifically, in some embodiments, the apparatus and methods are directed towards controlled delivery of micro-volumes of biomaterials into or onto a target location, the micro-volumes being defined as 0.001 mL-1 mL (or 1 μL-1,000 μL) of volume.