A61F2250/0091

COMPOSITE IMPLANT MATERIAL
20180000991 · 2018-01-04 ·

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.

PHOTON ENHANCED BIOLOGICAL SCAFFOLDING
20180008836 · 2018-01-11 ·

Provided herein are biocompatible scaffolds engineered to convey growth stimulatory light to cells and augment their growth on the scaffolds both in vitro and in vivo. Also provide are methods of modifying biocompatible transparent waveguides to control delivery of light from the waveguide material.

Midline Marker For Sling Implant

A sling assembly for treatment of stress urinary incontinence may comprise a midline marker, a sling, and a sleeve. The midline marker identifies the midpoint of the protective sleeve when it is installed on a transparent surface of the sleeve. The protective sleeve comprises a clear transparent surface and a colored opaque surface. During a procedure, the colored opaque surface of the sleeve provides contrast between the surfaces of the sleeve to identify any twisting present throughout the length of the sleeve. The clear transparent surface of the sleeve forms a channel at the center of the midline marker when the transparent surface of the sleeve is wrapped over the body of the midline marker. The channel is large enough for a surgical instrument to be inserted and cut the transparent surface to separate the sleeve from the midline marker after installation of the sling at a desired location.

ENDOTHELIAL OCULAR IMPLANT
20220401262 · 2022-12-22 · ·

An ocular implant is constructed of a clear, transparent, biologically compatible material and includes a hydrophilic outer surface configured for continuous attachment to a posterior surface of a cornea. The ocular implant has a first radius of curvature at initial attachment to the posterior surface of the cornea and a second radius of curvature at post-initial attachment to the posterior surface of the cornea. The first radius of curvature is different than the second radius of curvature. The ocular implant remains attached to the posterior surface of the cornea at both the first and second radii of curvature.

PROTECTIVE EYE SHIELD

A wearable medical device assembly for therapeutic treatment of a person includes: a wearable medical device configured to be applied over a portion of the person; a first anchor and a second anchor each comprising an adhesive configured to affix the respective anchor to the person's skin; and an attachment system that selectively attaches the wearable medical device to the first anchor and the second anchor, wherein the attachment system permits the wearable medical device to be detached from, and re-attached to, one or both of the anchors while both of the anchors remain affixed to the person's skin

Packaging and delivery device for a breast implant

Packaging for a breast implant, the packaging comprising a lid and a cavity, wherein one of the lid or the cavity is configured to provide direct delivery of the breast implant from the packaging to a surgical pocket. A method for the direct delivery of a breast implant from breast implant packaging to a surgical pocket, the method comprising the steps of: a. ensuring that a delivery device present in a lid or a cavity of the packaging is in a delivery position; b. forming an aperture in the delivery device, thereby opening the packaging; c. transferring the breast implant to the delivery device; d. positioning the delivery device in contact with the surgical pocket; and e. delivering the breast implant to the surgical pocket.

METHODS AND SYSTEMS FOR DIAGNOSIS AND TREATMENT OF A DEFINED CONDITION, AND METHODS FOR OPERATING SUCH SYSTEMS
20230111933 · 2023-04-13 ·

Disclosed herein, inter alia, are a method, system and a kit for improving a defined condition in a subject, the method comprising selecting a set of one or more correction zones, being surface zones on the surface of the subject's skin or defined angular zones in the subject's field of view, the one or more correction zones being associated with the condition; and placing the one or more correcting elements in said one or more correction zones to thereby cause improvement in said condition. Also provided herein are methods and systems for providing such correction zones related to a defined condition in a subject or to a defined cause in a subject being associated with a defined condition.

Compressible heart valve annulus sizing templates

Compressible heart valve annulus sizing templates suitable for minimally-invasive or otherwise reduced accessibility surgeries. The sizing templates may be folded, rolled, or otherwise compressed into a reduced configuration for passage through an access tube or other such access channel. Once expelled from the access tube the sizing templates expand to their original shape for use in sizing the annulus. The templates may be formed of an elastomeric polymer material such as silicone, a highly elastic metal such as NITINOL, or both. Grasping tabs or connectors for handles permit manipulation from outside the body. A NITINOL wireform may be compressed for passage through an access tube and expelled from the distal end thereof into a cloth cover to assume a sizer shape.

DSAEK corneal graft assemblies for optimized surgical operations
11654048 · 2023-05-23 · ·

Assemblies for storing, handling, transporting, viewing, evaluating, and/or shipping corneal tissue are provided. The assembly includes a corneal tissue carrier, optimized for DSAEK and UT-DSAEK corneal grafts, within a transport vial, the transport vial removably coupled to a stabilization base, wherein the ease of access to the graft carrier allows administering the corneal tissue sample to a patient in rapid succession so that more surgeries can be performed by a single surgeon in a single day.

NEGATIVE POISSON`S RATIO MATERIALS FOR INTRAOCULAR LENSES
20230149153 · 2023-05-18 ·

An intraocular lens includes a substantially circular lens element formed of a transparent material and one or more haptics extending outwardly from an outer edge of the lens element. The one or more haptics are formed of a polymer foam material having a negative Poisson's ratio (NPR) and are configured to couple the intraocular lens to an eye of a patient. The lens includes an inner region having a first index of refraction and an outer region disposed circumferentially surrounding the inner region, the outer region having a second index of refraction different from the first index of refraction.