A genital implant enhancement device and method is provided. The genital implant device comprises an elongated cylindrical sleeve that is configured to encircle a shaft of a penis and an external layer configured to cover one or more edges, surfaces, or layers of the sleeve to form one or more covered edges, surfaces, or layers themselves configured to align with the penis. One or more of the cylindrical sleeve and external layers may define one or more functional layers configured operative to be antibiotic and/or antimicrobial, anti-adhesive, slick and/or lubricious, anti-inflammatory, and/or fluid reducing. The device and method may be adapted for other sexual organs such as a clitoris, scrotum, testicles, and vaginal labia.

A penile implant enhancement device and method is provided. The penile implant device comprises an elongated cylindrical sleeve that is configured to encircle a shaft of a penis and an external layer. The elongated cylindrical sleeve is defined by one or more edges, surfaces, or layers, including a proximal edge, a distal edge, a first side, a second side, a top surface, and a bottom surface, and the external layer is configured to cover the one or more edges, surfaces, or layers of the sleeve to form one or more covered edges, surfaces, or layers. The covered edges, surfaces, or layers are configured to align with the penis. The method comprises the steps of administering one or more anesthetic agents; cutting a transverse incision above the pubic symphysis; clamping a lower edge of the transverse incision; dissection through the one or more layers of subcutaneous tissue to expose tunica albuginea; everting the penis; creating a pocket between the tunica albuginea and the skin; providing the aforementioned penile implant device; suturing the covered edges, surfaces, or layers to the penis; trimming the external layer, reverting the penis; and closing the transverse incision.

Devices and methods for inserting an implant into skin or other tissue of a patient can include an insertion device that can enclose and support a hyaluronic thread as it is injected into a patient's skin or other tissue. The device can include a cover member, a non-tubular support member, and the thread. The cover member can have a proximal portion, a closed distal portion, and an inner cavity extending from the proximal portion toward the closed distal portion. The thread can be positioned along a longitudinal length of support member, between the support member and the cover member. The non-tubular support member can extend within the inner cavity of the cover member. The cover member can be moveable relative to the support member to expose the thread.

Scaffolding constructs, medical devices comprising scaffolding constructs, and related methods of manufacturing and treatment are described. The scaffolding construct may comprise a biocompatible material, such as a polymer, copolymer, or hydrogel. The scaffolding construct may be porous and at least partially bioresorbable. Further, for example, the scaffolding construct may define a cavity for securing a medical implant therein.

The present invention relates to a thread embedding therapy rope and a thread embedding therapy needle apparatus comprising same, and disclosed are a thread embedding therapy rope and a needle apparatus comprising same, the rope comprising a linear core, which comprises a biodegradable polymer, and a metal wire, which is arranged to spirally encompass the outer circumferential surface of the linear core, wherein the metal wire comprises a biodegradable metal formed with magnesium or zinc as a main component, so as to have no side effects on biological tissue when applied to the human body by means of thread embedding therapy, pulling force on the tissue can be strengthened, lifespan can be extended over that of a conventional embedded thread of a biodegradable polymer, the drug loading capability of the embedded thread itself can be increased so as to allow for usefulness as a drug carrier, and a drug can be delivered through a simple method.

A prosthesis, radiation bolus, pre-surgical model, or burn mask formed using a rapid prototyping device, such as a three-dimensional printer. In some exemplary aspects, the prosthesis includes a scaffolding and a coating at least partially covering the scaffolding. Methods and systems for forming the prosthesis, radiation bolus, pre-surgical model, or burn mask are also provided.

A surgical device for correction of upper eyelid ptosis with autologous sling, comprising: a malleable rod (1), 6 cm long and 3 mm thick with blunt tapering tip (2); a catching end (3), where the catching end (3) contains both upper jaw (3A), lower jaw (38), where plurality of forward directed teeth (3C) positioned on both jaws inner surface; a hinge (3D) with closing spring, keeping both the jaws closed; an oval central hole (3E) of 2 mm positioned in mid of both the jaws so the upper hole faced towards the lower hole.

The device holds the sling and passes from one point of eyelid to the other in 5 seconds to 10 seconds.

Systems and methods are provided for altering the shape of a target tissue structure of a subject, e.g., a nasal septum or other nasal tissue that include securing a first end of a shaping element to tissue adjacent the structure; manipulating the tissue to alter a shape of the structure; and applying a force to the shaping element to maintain the altered shape of the structure.

The subject matter disclosed herein relates to an encoded cinching mechanism for use with an implant delivery sleeve. The delivery sleeve includes: an enclosure having a first portion, an orifice, and a throat disposed between the first portion and the orifice; and a cinching mechanism disposed about the throat, in which the cinching mechanism comprises a plurality of demarcations each of which are indicative of a sized opening of the throat.

Suture passer systems for tissue suspension and tissue compression are described. The system can include a shaft and a needle, wherein the needle is freely rotatable with respect to the shaft. The suture may include an overmolded segment. Methods of placing one or more implants, sutures, fastener, bone anchors and other devices are also described. The methods include moving tissue, including the superior pharyngeal constrictor muscle, palatopharyngeal arch, and palatoglossal arch. The methods include hyoid bone suspension.