Patent classifications
A61B2017/00526
SELF-ORIENTING ROTATING STENTRIEVER PINCHING CELLS
A clot removal device for removing a clot from a body vessel, the clot removal device including: an elongated member sized to traverse vasculature and having a proximal end and a distal end, the elongated member comprising a longitudinal axis; and an engagement structure connected to the distal end of the elongated member, the engagement structure comprising a plurality of pinching cells connected to each other, the at least one pinching cell being configured to engage clot in an expanded deployed configuration and to pinch the clot upon actuation to the clot pinching configuration, a first pinching cell of the plurality of pinching cells being connected to a second pinching cell of the plurality of pinching cells such that the second pinching cell is rotatable respective the first pinching cell substantially about the longitudinal axis.
Method of making diverging-light fiber optics illumination delivery system
A process of making a diverging-light fiber optics illumination delivery system includes providing a micro-post comprising a glass-ceramic light-scattering element that includes at least one of a ceramic, a glass ceramic, an immiscible glass, a porous glass, opal glass, amorphous glass, an aerated glass, and a nanostructured glass; and fusion-splicing the glass-ceramic micro-post to the optical fiber by pulling an arc between electrodes across a gap formed by the optical fiber and the glass-ceramic micro-post; maintaining the arc for a time sufficiently long to make facing surfaces of the optical fiber and the micro-post one of malleable and molten; and pushing and thereby fusing together the facing surfaces of the optical fiber and the micro-post. Some embodiments can include fusing the glass-ceramic micro-post to the optical fiber by applying a laser beam to heat up at least one of the facing surfaces of the optical fiber and the glass-ceramic micro-post.
Reduction splint for edentulous patients
An off-the-shelf oral splint that is operatively secured to the maxilla and mandible to assist in reduction and provide maintenance of reduction of maxillary and mandibular fractures in the edentulous or partially edentulous patient. The oral splint is fabricated into a plurality of standardized sizes. These sizes are determined by imaging a population of jaws, measuring dimensions thereof, manipulating (e.g., calculating the mean) these dimensions, and generating a size that is representative of a subset of that population. This can be done for all sizes that would represent individuals in that population. The splint itself is fabricated virtually by creating “U-shapes”, splitting them horizontally into halves, creating an evacuation channel, and generating a coupling mechanism to hold the halves together. The splint can then be printed or otherwise manufactured.
BIDIRECTIONAL FIXATION STEEL PLATE AND A BONE SHAFT FIXATION SYSTEM
The present invention relates to a bidirectional fixation steel plate and a bone shaft fixation system. The bidirectional fixation steel plate comprises a steel plate body, wherein the steel plate body is used to be implanted from a front side of a bone shaft and has a structure matched with the front side of the bone shaft to fixedly fit with a fracture end, the steel plate body is provided with at least two pairs of guide holes for first locking screws to pass through respectively in the structure matched with the front side of the bone shaft, and angles of the guide holes enable the first locking screws passing through to clamp an intramedullary nail together to control rotation and axial stability of the intramedullary nail. The bidirectional fixation steel plate proposed by the present invention may achieve support, anti-rotation and axial stability of the bone shaft fracture end through the cooperation of the first locking screws and the guide holes of the steel plate body provided with specific angles, to further enhance the reliability of fixation after reduction, thereby effectively guaranteeing to assist in stable reduction and healing of the fracture site.
Balloon Dilation Catheter for Use in Sinus Drainage Pathways
The present disclosure provides a balloon dilation catheter that includes a handle (102), a substantially rigid inner guide member (108) coupled to the handle, a shaft (118) arranged over the inner guide member, a balloon (120) coupled to the inner guide member, and a polymer ball tip (122) positioned at a distal end of the balloon. To treat a sinus drainage pathway of a subject using the balloon dilation catheter, the substantially rigid inner guide member is positioned into the drainage pathway of the sinus of the subject via a nasal passageway. The balloon is then inflated to expand or otherwise remodel the drainage pathway.
STENT, STENT PRECURSOR PRODUCTION DEVICE, AND STENT PRODUCTION METHOD
In this stent, two superelastic fine wires are disposed along the axial direction at a prescribed helical pitch so as to have a prescribed stent inner diameter D0, while a pair is formed between two helical fine wires that are disposed across a micro gap of a size not more than five times the wire diameter of the fine wires in such a manner as to include a mutually contacting state. A prescribed reticulation gap is formed by crossing a clockwise-wound helical fine wire pair and a counterclockwise-wound helical fine wire pair in a plain-woven fashion, so as to have an axial gap equal to [(prescribed helical pitch)−{2×(fine wire diameter)}−(micro gap)] and a circumferential gap equal to [{(stent inner circumferential length corresponding to stent inner diameter)/N}−{2×(fine wire diameter)}−(micro gap
Vibrational catheter devices and methods for making same
A method for making a vibrational catheter device includes providing a transition connector comprising a proximal portion, a distal portion, and a tapered portion that defines a tapered outer surface of the transition connector, the proximal portion being wider than the distal portion, and the transition connector having a bore disposed within the tapered portion; inserting a proximal end of an ultrasound transmission member into the bore; and deforming at least part of the transition connector at the tapered outer surface so as to apply greater force to the wider proximal portion than to the distal portion to secure the proximal end of the ultrasound transmission member within the bore.
Braided medical device and manufacturing method thereof
An medical implantable occlusion device (100) is disclosed having a collapsed state and an expanded state and comprising a braiding (101) of at least one thread, and a distal end (102) comprised of said braiding. The distal end comprises loops (103, 104, 204, 304) formed by loop strands (105, 106, 206, 306) of the at least one thread, wherein, at least in said expanded state, each loop strand has a curved shape and extends away from a centre point (117) of the distal end, whereby an apex point (107, 108, 208, 308) of each of the loop strands corresponds to the turning point of the curved shape and to the point of each of the loop strands being arranged closest to the centre point. At least one of the loop strands is displaced from the centre point by a centre distance (109, 110, 210, 310), and the apex point lie at a distance from a periphery (113) of the distal end.
Surgical end effector assembly including a connector strip interconnecting a plurality of staples
A surgical staple cartridge is disclosed comprising a plurality of staples removably stored within the surgical staple cartridge. The staples comprise staple legs which extend from a staple base portion. The staple legs comprise staple tips configured to pierce tissue and contact a corresponding forming pocket of an anvil of surgical stapling instrument. The staples further comprise zones having different hardnesses.
Treatment instrument and manufacturing method of treatment instrument
A treatment instrument including a heat transmitter that includes a treating surface and an installation surface, a substrate attached to the installation surface, and a heat generator formed on a surface of the substrate. The substrate surface and heat generator together form an uneven surface. First and second adhesion layers formed of a material having thermal conductivity and electrical insulation are provided between the installation surface and the substrate. The first adhesion layer is in close contact with the installation surface, and the second adhesion layer is in close contact with the heat generator and the substrate surface. The second adhesion layer is inserted into a recess in the uneven surface formed by the heat generator on substrate surface so as to increase the contact area between the second adhesion layer and the uneven surface.