A device for inserting a pre-filled or silicone prosthesis into a surgical pocket is formed from a sleeve formed of a bottom layer and a top layer attached to the bottom layer along longitudinal edges of the bottom layer and top layer. The top layer has a greater width than the bottom layer so as to form a half-cylinder shape when the sleeve is filled. The sleeve has a constant cross-sectional area along a length of the sleeve. This device reduces the chances for the implant to rotate in an unintended manner due to the non-circular cross-section of the sleeve.

A prosthetic implant with improved properties, suitable for implantation to the human body, comprising a composite comprising a base material and a plurality of additives, wherein the additives are selected from radiolucent additives and/or hyperechoic additives; or wherein the additives are selected to reduce the solvent concentration by between 5%-95%; or wherein the additives are selected to increase the elastic modulus by more than 20%; or wherein the additives are selected for combining these effects.

A prosthetic insertion apparatus and related methods of use in delivering filled prosthetic bladders through a skin incision and into a surgical cavity or pocket. The prosthetic insertion apparatus imparts control and retention properties to a surgical professional such the prosthetic bladder can be oriented and manipulated into the surgical cavity without risk of inadvertent dropping of the prosthetic bladder and without imparting damaging stress or torque to the bladder. Suitable materials can be utilized that are selected as having advantageous properties including lubricity, rigidity, easily sterilizable, and high strength.

Provided are a vascular stent, a conveying balloon thereof, and an implanting system. The vascular stent comprises a flexible light-transmitting body. The flexible light-transmitting body is provided with a hardenable channel. The hardenable channel is arranged in the circumferential direction and the axial direction of the flexible light-transmitting body. The hardenable channel is used for filling a liquid photocuring supporting material, and the liquid photocuring supporting material is cured after being illuminated so as to radially support the flexible light-transmitting body.

A drainage device for use in an eye to drain aqueous humour so as to reduce intraocular pressure or for treating glaucoma. The device has a multi-lumen tube having a first end, a second end opposite the first end, and a plurality of lumen extending between the first end and the second end. At least one of the lumen is sealed at the first end. A flow through the multi-lumen tube is adjusted by forming at least one aperture open in one of the lumen through a wall of the tube and/or sealing at least one aperture open in one of the lumen. The tube has a longitudinal axis through the first end and the second end, and an outer surface extending between the first end and the second end. A cross-section perpendicular to the longitudinal axis has a non-circular shape at the outer surface with an aspect ratio of at least 3:1.

A device for inserting a pre-filled or silicone prosthesis into a surgical pocket is formed from a sleeve formed of a bottom layer and a top layer attached to the bottom layer along longitudinal edges of the bottom layer and top layer. The top layer has a greater width than the bottom layer so as to form a half-cylinder shape when the sleeve is filled. The sleeve has a constant cross-sectional area along a length of the sleeve. This device reduces the chances for the implant to rotate in an unintended manner due to the non-circular cross-section of the sleeve.

An open, seal-less intraocular lens is disclosed herein. An example intraocular lens may include an annular substrate including an oil electrode disposed in or on an inner sidewall of the annular substrate to electrostatically manipulate a volume of electrowetting oil, an optical window coupled to the substrate, where a side of the optical window adjacent to the inner sidewall and the inner sidewall of the annular substrate define a region for constraining the volume of electrowetting oil, and a saline electrode coupled to the annular substrate, the saline electrode positionable within an aqueous humor of an eye upon implantation

The present invention provides an instrument for ear treatment that facilitates treatment or surgery in the ear by inserting a tool, such as a scalpel, into the instrument for ear treatment. An instrument 1 for ear treatment of the present invention includes an insertion portion 2 formed in a horn tubular shape and configured to be inserted into an external acoustic meatus, wherein a support portion 3 configured to support a tool to be inserted into the insertion portion 2 is provided on an inner circumferential surface 2a or at an open end on a distal end side of the insertion portion 2. The support portion 3 is preferably formed from a projection projecting from the inner circumferential surface 2a of the insertion portion 2 and the support portion 3 is preferably formed on a distal end side in a direction of an axis L1 of the insertion portion 2.

The invention relates to a device (1) and method for selecting the size and shape of a prosthesis and/or for determining the location of marks to be made on the external face of the skin of a patient intended to receive such a prosthesis, for example for repairing a hernia, comprising a sheet (2) of transparent material, the said sheet comprising: a plurality of graphical representations (3a, 3b, 4a, 4b, 5a, 5b, 5c, 5d) concentrically embodying the respective outlines of various shapes and sizes of prosthesis, a plurality of first holes (6a, 6b, 6c, 6d, 6e, 7a, 7b, 7c, 7d, 7e) arranged along the transverse line passing through the centre of the said sheet, and a plurality of second holes (8a, 8b, 8c, 8d, 8e, 8f, 8g, 9a, 9b, 9c, 9d, 9e, 9f, 9g) arranged along the longitudinal line passing through the centre (C) of the said sheet.

A prosthetic implant with improved properties, suitable for implantation to the human body, comprising a composite comprising a base material and a plurality of additives, wherein the additives are selected from radiolucent additives and/or hyperechoic additives; or wherein the additives are selected to reduce the solvent concentration by between 5%-95%; or wherein the additives are selected to increase the elastic modulus by more than 20%; or wherein the additives are selected for combining these effects.