An intraluminal stent (1) and a preparation method therefor are provided. The intraluminal stent (1) includes at least one sub-stent. The sub-stent includes at least a first wire (4) extending along a first spiral direction and at least a second wire (5) extending along a second spiral direction, and the first wire (4) and the second wire (5) extend in different directions to form several wire intersection points. The intraluminal stent (1) has several wrapped portions (2) to wrap two corresponding wire tail ends. A wrapping connector (3) is disposed at a periphery of the wrapped portion (2). Two end portions of the wrapping connector (3) are firmly connected to regions corresponding to two ends of the wrapped portion (2). The two wire tail ends of the wrapped portions (2) are wrapped by using the wrapping connector (3). The stent (1) is less harmful to intraluminal tissues and a relatively strong tensile resistance.

Systems for bone fracture repair are disclosed. One system includes a biocompatible putty that may be packed about a bone fracture to provide full loadbearing capabilities within days. The disclosed putties create an osteoconductive scaffold for bone regeneration and degrade over time to harmless resorbable byproducts. Fixation devices for contacting an endosteal wall of an intramedullary (IM) canal of a fractured bone are also disclosed. One such fixation device includes a woven elongated structure fabricated from resorbable polymer filaments. The woven elongated structure has resilient properties that allow the woven structure to be radially compressed and delivered to the IM canal using an insertion tube. When the insertion tube is removed, the woven structure expands towards its relaxed cross-sectional width to engage the endosteal wall. The woven elongated structure is impregnated with a resorbable polymer resin that cures in situ, or in the IM canal.

A cup and a temporary insert are respectively configured to be tightly press fitted into each other along their periphery. The temporary insert includes a through hole communicating outside with a free space between the outer surface of the temporary insert and the inner surface of the cup. In the through hole can be engaged the threaded end of an impactor, for manipulating the cup when it is being set. A syringe can be engaged, enabling a liquid under pressure to be injected into the free space, thus separating the temporary insert from the cup without any risk of damaging the inner surface of the cup. Thus, the cup can be securely manipulated when it is being set without any risk of damaging the inner surface of the cup.

A stent and method of making incorporating flexible, preferably polymeric, connecting elements into the stent wherein these elements connect element(s) across an intervening space. The polymeric connecting elements are designed to fold within the space between the outer diameter of the stent and the inner diameter of the stent.

A stent for aorta is formed by weaving at least two types of filaments having different diameters, such as a first filament and a second filament. The stent is configured to be at least partially compressible and extensible along the axial direction of the stent in a natural release state, wherein the first filament has a diameter of 20-150 μm, and the second filament has a diameter of 150-800 μm. When the stent is used in the treatment of aortic aneurysm and/or aortic dissection lesions, due to the axial compressibility and extensibility of the stent, low liquid permeability and strong radial support force are provided where needed in the aorta, and due to the axial stretchability thereof, the stent can be easily assembled to a delivery system having an appropriate diameter. Also provided are a stent kit comprising the stent and a stent delivery system.

A stent, for use in an aorta, is characterized in that the stent is at least made of a first wire and a second wire of different diameters by means of weaving, and the stent is configured to be at least partially compressible and extensible in the axial direction of the stent in a natural release state, wherein the first wire has a diameter of 20-150 μm, and the second wire has a diameter of 150-800 μm. When the stent is used in the treatment of aortic aneurysm lesions and/or aortic dissection lesions, the stent provides low fluid permeability and a strong radial support force at the desired site in the aorta by means of the axial compressibility and extensibility of the stent, and is easily assembled into the delivery system having a suitable diameter. Further provided are the stent kit comprising the stent, and the stent delivery system.

Proposed is an aqueous humor drainage device with an adjustable tube diameter that is inserted into an eyeball to drain aqueous humor discharged from the eyeball to the outside, the aqueous humor drainage device comprising: an annular outer tube part having a predetermined thickness and having a hollow inside; and an annular inner tube part coupled to the inner surface of the outer tube part and having a predetermined thickness and a hollow inside, wherein the inner tube part has a shrinkage hole formed therein and is made of a biodegradable material.

Accommodating intraocular lenses and methods of use. The accommodating intraocular lenses include peripheral regions that are adapted to be more responsive to certain types of forces than to other types of forces. For example, the accommodating intraocular lenses can include haptics that are stiffer in an anterior-to-posterior direction than in a radial direction.

A hydraulic muscle comprises a hollow carbon nanotube (CNT) yarn tube comprising: a plurality of CNT sheets twisted and wrapped in form of a hollow tube; and a binding agent infiltrated in the plurality of CNT sheets that binds the plurality of the CNT sheets together. A method of manufacturing a hydraulic muscle comprises: twisting and wrapping a plurality of carbon nanotube (CNT) sheets around a core fiber; infiltrating a binding agent in between the plurality of CNT sheets, wherein the binding agent binds the plurality of the CNT sheets together; and removing the core fiber from the plurality of CNT sheets.

The present technology is directed to an adjustable power intraocular lens comprising a container, an optical fluid in the container, and a transport substance in solution with the optical fluid. The container has an optical component and a peripheral component extending around at least a portion of the optical component. The optical component has an anterior optical element, a posterior optical element, and a fluid chamber having a chamber volume between the anterior optical element and the posterior optical element. The transport substance is configured to pass through the container. The adjustable power intraocular lens further comprises volume control elements in the container. The volume control elements are configured to be activated by a non-invasive energy and upon activation release the transport substance into the optical fluid to decrease the chamber volume and/or absorb the transport substance from the optical fluid to increase the chamber volume.