Abstract: A vehicle door cover device for inhibiting contact between an upper frame portion of a door frame of a vehicle door assembly and a glass pane during installation of the glass pane into the vehicle door assembly includes a first sidewall, a second sidewall, and a channel wall that extends between the first sidewall and the second sidewall. The first sidewall, the second sidewall, and the channel wall form a pillar receiving channel that extends between the first sidewall and the second sidewall, and the pillar receiving channel comprises a width dimension and a length dimension and the width dimension is sized to slidably receive the upper frame portion of the door frame during installation of the glass pane.

Abstract: A syncing apparatus for synchronizing a process dolly to a conveyor includes a mounting frame and a sync arm. The mounting frame is configured to be mounted to a frame of the process dolly. The sync arm is coupled to the mounting frame and includes a wheel and a biasing member coupled to the wheel and configured to bias the wheel to an extended position. The wheel is configured to contact a contact feature of the conveyor to synchronize the process dolly to a movement of the conveyor when biased to the extended position. Compression of the biasing member moves the wheel to a retracted position wherein the wheel is configured to traverse the contact feature of the conveyor and the process dolly is unsynchronized from the movement of the conveyor.

Abstract: A vehicle door cover device for inhibiting contact between an upper frame portion of a door frame of a vehicle door assembly and a glass pane during installation of the glass pane into the vehicle door assembly includes a first sidewall, a second sidewall, and a channel wall that extends between the first sidewall and the second sidewall. The first sidewall, the second sidewall, and the channel wall form a pillar receiving channel that extends between the first sidewall and the second sidewall, and the pillar receiving channel comprises a width dimension and a length dimension and the width dimension is sized to slidably receive the upper frame portion of the door frame during installation of the glass pane.

Abstract: Medical devices such as catheters can include structure or provision that permit a physician or other health care professional to adjust the stiffness of at least a portion of the medical device. In some instances, the medical device may be adjusted prior to inserting the medical device into a patient. In some cases, the medical device may be adjusted while in use within the patient.

Abstract: A prosthetic heart valve includes a collapsible stent and a valve assembly disposed within the stent. A first cuff is disposed adjacent the stent. A filler is annularly disposed about the stent radially outward of the first cuff and radially outward of the stent. The filler has a first circumferential layer with a first inner wall, a first outer wall, and a plurality of first ribs connecting the first inner wall to the first outer wall. The filler has an expanded condition in which the first inner wall is spaced a first distance from the first outer wall in a radial direction transverse to the longitudinal direction of the stent, and a collapsed condition in which the first inner wall is spaced a second distance from the first outer wall in the radial direction, the first distance being greater than the second distance.

Abstract: Medical devices such as catheters can include structure or provision that permit a physician or other health care professional to adjust the stiffness of at least a portion of the medical device. In some instances, the medical device may be adjusted prior to inserting the medical device into a patient. In some cases, the medical device may be adjusted while in use within the patient.

Abstract: Medical devices such as catheters can include structure or provision that permit a physician or other health care professional to adjust the stiffness of at least a portion of the medical device. In some instances, the medical device may be adjusted prior to inserting the medical device into a patient. In some cases, the medical device may be adjusted while in use within the patient.

Abstract: Medical devices such as catheters can include structure or provision that permit a physician or other health care professional to adjust the stiffness of at least a portion of the medical device. In some instances, the medical device may be adjusted prior to inserting the medical device into a patient. In some cases, the medical device may be adjusted while in use within the patient.

Abstract: A medical implant includes a metallic base, a tie layer, and at least a first layer overlying an outer surface of the tie layer. The tie layer is bonded to at least a portion of a surface of the metallic base. The tie layer includes magnesium or a magnesium-based alloy. The tie layer can have an outer surface comprising dendritic grains. The tie layer can have a rough outer surface defined by pores, projecting grain structures, and/or projecting particles. A method of producing a tie layer on a medical device includes applying magnesium or a magnesium-based alloy to the medical device and cooling the magnesium or the magnesium-based alloy to produce a rough outer surface.

Abstract: A delivery system has a stent and a balloon. The stent has a first section made of a plurality of interconnected framework members which define a plurality of potential side branches. The balloon is a dual lumen balloon that can inflate from the proximal end to the distal end with a plurality of protrusions and/or herniations.

Abstract: Described herein are implantable medical devices for delivering a therapeutic agent to the body tissue of a patient, and methods for making such medical devices. In particular, the implantable medical devices, such as intravascular stents, have a coating which includes at least one coating composition and has an exposed abluminal surface and an exposed luminal surface or exposed side surface.

Abstract: Among other things, a bio-erodible implantable endoprosthesis comprises a member that includes (a) a core having a surface, and (b) a bio-erodible metal on a least a portion of the surface of the core, wherein the bio-erodible metal erodes more slowly than the core and includes openings through which physiological fluids can access the core upon implantation.

Abstract: Medical devices such as catheters can include structure or provision that permit a physician or other health care professional to adjust the stiffness of at least a portion of the medical device. In some instances, the medical device may be adjusted prior to inserting the medical device into a patient. In some cases, the medical device may be adjusted while in use within the patient.

Abstract: A stent may comprise a plurality of serpentine bands, wherein adjacent serpentine bands are connected by at least one connector strut. A serpentine band may comprise alternating straight struts and s-shaped struts. Connector struts may comprise first connector struts and second connector struts, wherein the first connector struts are nonparallel to the second connector struts.

Abstract: In at least one embodiment, a stent comprises an expandable framework comprising a plurality of serpentine bands and a plurality of connector struts. Each serpentine band comprises a plurality of alternating struts and turns. A plurality of the serpentine bands each have their proximal turns aligned on a common stent circumference and comprise first distal turns and second distal turns. The first distal turns are aligned with one another on a common stent circumference. The second distal turns aligned with one another on another common stent circumference. Each band in the plurality comprises first struts and second struts. Each first strut is attached between a proximal turn and a first distal turn, and each second strut is attached between a proximal turn and a second distal turn. The second struts are wider than said first struts.

Abstract: In at least one embodiment, a stent includes an unexpanded configuration, a nominally expanded configuration, and a fully expanded configuration. The stent further includes a plurality of circumferential bands and a plurality of connectors connecting adjacent circumferential bands to one another. Each circumferential band has a plurality of struts interconnected by bridges. Adjacent struts form strut pairs and are connected to one another at a first end or a second end but not both. Each strut pair defines an opening between the struts of the strut pair; the bridges extend into the openings. In the unexpanded configuration, the struts are straight along their length. Also in the unexpanded configuration, the bridges include two adjacent straight segments that are connected by a u-shaped segment, and the straight segments are parallel to one another and to the longitudinal axis of the stent.

Abstract: A stent may include a side branch cell comprising a plurality of petals. Each petal may comprise struts and turns, and may have a longitudinal axis oriented at an angle to the stent longitudinal axis. Each petal may comprise a plurality of struts and at least one turn. For each petal, the width of a turn may be greater than the width of the struts. Upon expansion of the stent, a petal may deploy outwardly in a stent radial direction beyond an outer diameter of the rest of the stent.

Abstract: A bifurcated stent that uses telescoping rings to support or form the side branch lumen. This design allows the bifurcation branch to extend easily, to a useful distance, and to be deployed along oblique angles. Best of all, this design avoids the need to deploy a bent stent.

Abstract: A stent has a plurality of expansion columns that extend in a radial direction to form a circumference of the stent and interconnected in the axial direction to form an overall axial length of the stent. Each expansion column has a plurality of first cells and a plurality of second cells that alternates along the expansion column with at least one first cell. Each first cell has at least two facing walls extending in the radial direction that have a first width. The second cells each have at least two facing walls that extend in the radial direction which have a second with greater than the first width. The first cell uses less force to open than the second cell, but upon opening provides increased radial strength by creating a substantially vertical cell wall.

Abstract: A stent assembly comprises a second stent body and a substantially tubular first stent body defining a first lumen and containing a side branch opening. In an undeployed state, the second stent body is at least partially comprised of rings having peaks and valleys at least some of the valleys of adjacent rings being interconnected by bridges. In an expanded state, the rings of the second stent body define a second lumen opening in fluid communication with the first lumen. The second lumen has superior body vessel coverage and is flexible enough to form an oblique angle relative to the longitudinal axis of the first stent body.