Embodiments of the invention include a breast nipple areola complex tattoo stencil comprising first, second and third stencil sections. The first stencil section defines an areola area. The second stencil section defines a nipple area and tubercle areas. One or more registration elements on the first and/or second stencil sections enable registration of the second stencil section to the first stencil section. The third stencil section defines one or both of a nipple shading area and a nipple highlight area. One or more registration elements on the third and/or second stencil sections enable registration of the third stencil section to the second stencil section.

The breastfeeding device present in the invention, simulates natural breastfeeding experience and delivers fluid, milk or infant formula to the nursing infant in a contactless or latch free manner than any prior art in this field. This device integrates physical sensors to the breastfeeding device and includes a neck strap, refillable housing chamber that contains fluid, a tubing that connects the housing chamber to a prosthetic nipple via a sealing attachment and a prosthetic nipple for infant latching to nurse. The invention is a notable step forward in creating an effective, safe and contactless nursing which mitigates and prevents bruised, sore nipples or engorged breasts.

An anatomically accurate device of a human areola and nipple is provided for in the present invention.

The invention relates to a biological prosthesis (10) consisting of a nipple-areola complex belonging to the family of pigs, cattle or goats, said nipple-areola complex having been treated for use in humans.

The present disclosure relates to surgical grafts for replacing nipples and areolas lost to disease or trauma with surgical grafts of decellularized donor nipples and areolas and to placing and recellularizing such grafts. The disclosure further provides methods for decellularizing epidermis. The decellularized epidermis can be used as a protective cover for skin wounds.

Apparatus and methods for nipple and breast formation are described where devices precondition or expand a target nipple tissue to reduce the pressure exerted by the skin on an eventual implant. Generally, the apparatus comprises a mold having a contact surface which is cured in conformance with a breast upon which the mold is positionable, the contact surface having an adhesive for securement upon the breast, and the mold defining a cavity along the contact surface which conforms to a size of a nipple to be formed upon the breast and where the cavity further comprises the adhesive for securement to the nipple. A breast enlargement device comprises a cup larger than the target breast and further defines an inner surface which adheres to the breast when contacted.

Apparatus and methods for nipple and breast formation are described where devices precondition or expand a target nipple tissue to reduce the pressure exerted by the skin on an eventual implant. Generally, the apparatus comprises a mold having a contact surface which is curved in conformance with a breast upon which the mold is positionable, the contact surface having an adhesive for securement upon the breast, and the mold defining a cavity along the contact surface which conforms to a size of a nipple to be formed upon the breast and where the cavity further comprises the adhesive for securement to the nipple. A breast enlargement device comprises a cup larger than the target breast and further defines an inner surface which adheres to the breast when contacted.

A nipple implant assembly and method for implanting the nipple implant are provided. The nipple implant assembly comprise of nipple skeleton with or without areola made of metallic or non-metallic memory-shape bio-compatible material. The nipple implant assembly may consist of holes to allow growth of natural breast tissue into the implant for improved holding better attachment of the implant into the human's tissue. The nipple implant assembly may be coated by or cast in a polymeric coating.

A method for fabricating a pacifier having surface features replicating those of a nursing mother's nipple, wherein the nipple has a length, the method including steps of utilizing the nursing mother's nipple as a positive mold to cast a first negative mold; utilizing the first negative mold to cast a replica of the nursing mother's nipple; modifying the replica of the nursing mother's nipple so that said replica has a length greater than that of the nursing mother's nipple; utilizing the modified replica of the nursing mother's nipple as a second positive mold to cast a second negative mold; and utilizing the second negative mold to cast an extended length replica of the nursing mother's nipple.

A breast prosthesis includes a cured silicone rubber skin layer having a shape corresponding to a natural breast and defining a cavity therein. A cured silicone substance is disposed in the cavity. In a method of making a breast prosthesis, a mold that defines a breast-shaped cavity therein is generated. A silicone rubber skin material is applied to the cavity. The silicone rubber skin material in the cavity is cured to form a skin layer. A low-oil silicone gel or a no-oil silicone gel is injected into the cavity inside of the skin layer. The low-oil silicone gel or a no-oil silicone gel is cured so as to generate the breast prosthesis. In another method of making, a barrier layer is applied to the skin layer and a silicone oil is injected into the cavity inside of the barrier layer prior to curing.