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.

A breast milk pump includes a breast interface member which has an inner cavity through which milk can flow, and a negative pressure assembly in fluid communication with one side of a diaphragm. An opposite side of the diaphragm is in fluid communication with the inner cavity. The diaphragm separates the inner cavity from the negative pressure assembly. A suckling assembly includes a tongue member and an actuator coupled to the tongue member for causing movement of the tongue member. A tongue position adjustment assembly is coupled to the suckling assembly and operative to cause displacement of the suckling assembly with respect to an inner surface of the inner cavity.

The present disclosure is directed to an improved electric breast pump performance by providing independent adjustment of pumping parameters, such as vacuum and cycle, among others, for each breast when double pumping. The electric breast pump provides the capability to independently select discrete values for each breast so that a separate setting can be set for vacuum and/or cycles or both and can be selected for each breast. These separate settings can be varied and adjusted independently. The improved breast pump can be operated to pump individual breasts, or both breasts simultaneously according to the setting. The improved breast pump utilizes data and information received from previous breast pump sessions to determine and provide improved and optimal settings for future sessions, thereby creating a more efficient breast pump system.

A therapeutic device is placed over the breast and improves the quality of breastfeeding experience, aiming to heal and treat specific ailments nursing mothers encounter. The breast care device allows the user to maintain treatment while allowing for mobility during therapy. One aspect of the breast care device is made to contain and distribute therapeutic fluids, which are known to soothe breast pain, nipple cracks, anatomical variations, thrush, bites, milk blister, and other ailments. Another aspect of the breast care device contains an array of light elements for the purpose of light therapy, aiming to soothe the same ailments. The final aspect of the breast care device can contain a variety of electrical components, such as rollers for massage, vibration mechanisms for therapy, or ultrasound for imaging or therapy.

The present invention provides a supplemental nutrition apparatus. The supplemental nutrition apparatus may comprise a reservoir coupled to and in fluid communication with a fluid passageway, wherein the fluid passageway is configured to communicate fluid from the reservoir to a fluid passageway outlet, and a support element configured to engage a user, to at least partially support the fluid passageway, and to position the fluid passageway outlet proximate to the user's nipple.

A negative pressure wound dressing for use with breast incisions. The wound dressing includes a drape layer, a manifold layer, a base layer, and a reduced pressure interface. The drape layer has a first surface and a second, wound-facing, surface. The drape layer is substantially impermeable to liquid and substantially permeable to vapor. The manifold layer has a first surface and a second, wound-facing surface. The manifold layer has a perimeter defined by a first convex curved side surface defining a first lobe, a second convex curved side surface defining a second lobe, and a connecting portion between the first lobe and the second lobe. The base layer is configured to: (i) couple the drape layer to the manifold layer, and (ii) the dressing to a patient's tissue. The reduced pressure interface is integrated with the drape layer.

A method for facilitating milk extraction from a female breast may involve applying a breast contacting portion of a breast pump system to a breast, activating the breast pump system to administer multiple breast pumping cycles, and applying vibrations to the breast during at least a portion of each of the breast pumping cycles, using a vibration device. A vibration generating device may be a component of a breast pump system, an added attachment on a breast pump system or a separate component that works in conjunction with a breast pump system.

An apparatus for biomimetic expression of breast milk can comprise a breast interface having an expandable membrane configured to mimic the geometry of an infant's mouth. Various regions of the expandable membrane may be configured to simulate the structure and/or function of various parts of an infant's mouth. The expandable membrane may comprise one or more of a distal sealing region configured to simulate the lips, a superior region configured to simulate the hard palate, an inferior protruding region configured to simulate the gums, an intermediate curved region configured to simulate the tongue, and one or more internal expansion regions configured to simulate the soft palate and the throat. The expandable membrane may have a varying thickness throughout the one or more various regions to enable movement of the regions similar to the movement of the corresponding regions of an infant's mouth during nursing.

Systems, kits and methods for preparing an injection system and/or treating target lesions with a selective internal radiation therapy which includes a double-barrel syringe loaded with a two-component tissue glue and radioisotope loaded microspheres. The microspheres are loaded into the syringe based on the size of the target location and are administered with a needle or dual-lumen catheter. Dosing regimens for treating breast cancer lesions or surgical beds up to 130 mm in diameter and hepatocellular carcinoma lesions up to 50 mm are included.

A tissue expander can be configured to collect extracellular fluid from within a patient’s body cavity. The tissue expander can be implanted into a subdermal cavity during a procedure, such as a breast reconstruction procedure, and facilitate the expansion of the subdermal cavity in preparation for placement of a final implant.