Merit Medical Systems, Inc.

Momentum Medical Corp.

Darla R Gill

Zeke Eller

Trent Clegg

Rich Snider

Jerrold L Foote

Fred P Lampropoulos

Jim D Mottola

Jeremy W Snow

Thomas Patrick Robinson

William Padilla

Bryan K Elwood

Barton P Gill

Diana Anca

Gregory R McArthur

Randall D Block

Fred P Lampropolous

Faiz Bhora

Tom Robinson

Brenda Lyons

Faiz Bohra

Delivery systems and methods for deploying an implantable device are disclosed, which can include a delivery device having an outer tubular member and an inner assembly. The inner assembly is disposed within and is slidably movable relative to the outer tubular member. The inner assembly can include a pusher at a distal portion. The pusher abuts and restricts proximal movement, relative to the inner assembly, of a crimped implantable device within the outer tubular member. The pusher can include a slot to accommodate a suture binding mechanism of the implantable device. The delivery device can include a tip disposed at a distal end. The tip includes a tip transition zone. The inner sheath and outer tubular member can each have sections of distinct rigidity along their lengths with transition zones between the sections. A transition zone of the outer tubular member and a transition zone of the inner sheath can be longitudinally offset.

Implantable device delivery system

Implantable device embodiments, such as stents, and particularly esophageal stents, formed of a scaffolding structure are disclosed. The scaffolding structure is formed of one or more strand elements arranged in a braided pattern. A covering may coat the scaffolding structure. A valve can be secured to the scaffolding structure and/or the covering. Anti-migration features may be formed by bends in the one or more strand elements. The bends forming the anti-migration features protrude outwardly away from an outer surface of the implantable device.

Esophageal stent

A stent comprised of a scaffolding structure having components configured to allow at least a portion of the stent to decrease in diameter in response to an axial force applied to the stent. Further, the components and elements of the stent may be configured to balance transverse forces applied to the stent, thus reducing the incidence of infolding.

A stent comprised of a valve and a scaffolding structure having components configured to allow at least a portion of the stent to decrease in diameter in response to an axial force applied to the stent. Further, the components and elements of the stent may be configured to balance transverse forces applied to the stent, thus reducing the incidence of infolding.

Esophageal stent with valve

Stent embodiments formed of a scaffolding structure are disclosed. Some embodiments may include a valve. A portion of the scaffolding structure may include a lattice structure formed by a plurality of interconnected arms arranged to form quadrilateral-shaped cells, such as diamond-shaped cells. The scaffolding structure may be formed by rows of strut arms arranged as annular segments and adjacent annular segments interconnected by connectors that extend in the longitudinal direction. The scaffolding structure may also be formed by rows of strut arms arranged in a helical pattern. The scaffolding structure has components configured to allow at least a portion of the stent to decrease in diameter in response to an axial force applied to the stent. Further, the components and elements of the stent may be configured to balance transverse forces applied to the stent, thus reducing the incidence of infolding.

The embodiments disclosed herein relate to lockable syringe assemblies and related devices and methods. The syringe assembly may include a barrel, a plunger, and a locking mechanism. In some arrangements, the locking mechanism is an elastomeric locking ring or a rigid partial ring. The plunger may include a plurality of ribs and is longitudinally moveable within the barrel. Once the plunger is disposed at a desired longitudinal location, the plunger can be axially rotated and locked in such a way that further longitudinal movement is restricted.

Lockable syringe assemblies and related devices and methods

Various embodiments of mouthpieces for use during endoscopic procedures are disclosed herein. According to various embodiments, a mouthpiece may include a shield, a primary instrument channel, a bite block, an oxygen administration channel and a tongue depressor. The shield, bite block, oxygen administration channel and tongue depressor may be integrally formed.

Mouthpiece and methods of use of same

Apparatus, systems, and methods are provided for deploying an implantable device, such as a stent, within a lumen of a body of a patient. The delivery device may include an inner member and an outer sheath surrounding a distal portion of the inner member and configured to retain the implantable device sheathed near the distal end of the outer sheath until deployment. The outer sheath is slidably moveable relative to the inner member such that proximal movement of the outer sheath relative to the inner member deploys the implantable device. A trigger assembly of the delivery device can include an internal connector coupled to the outer sheath, a plurality of triggers, and a floater coupling two of the triggers. The triggers are serially retracted to deploy the stent. A panchor secures the stent against proximal and distal movement relative to the inner member during deployment.

Stent delivery systems and methods

A dual handled walking-assist and uprisal-assist device is disclosed having the handles spaced at a predetermined distance to provide a stable structure for rising from and lowering to a seated position, in addition to serving as a walking aid. The walking- and uprisal-assist device has a structure having a first handle or first pair of handles which are useful whenever a user is in a standing position. A second handle or second pair of handles are spaced a preselected distance from the first handle or handles and at a preselected distance from the bottom of the device. An infirmed user can use the second handle or handles as a grip to push against when the user is rising from a chair. The second handle or handles are connected to one or more load-bearing shafts and the geometrical centers of the handles are positioned relative to the load-bearing shafts to provide a stable structure when used for uprisal and walking. The load-bearing shaft or shafts of the device may be configured with height adjustment means to selectively determine the overall height of the device. The walking- and uprisal-assist device of the present invention may be manifest in either a cane or a walker.

Dual handled walking and uprisal assist device

An electronically controlled syringe system for connection to a balloon catheter or other balloon-type member and for automatically monitoring, displaying and recording inflation data when the syringe system is used to inflate the balloon catheter or other balloon-type member. A syringe having a barrel and a syringe plunger is selectively operable to increase fluid pressure applied to the balloon catheter or other balloon member by sliding the plunger further into the barrel. Positive pressure applied to the balloon catheter or member can be released by withdrawing the syringe plunger toward the rear of the barrel. A piezoresistive semiconductor transducer housed on the barrel of the syringe senses positive fluid pressure applied by the syringe. The electric signal output by the transducer is input to a controller where the signal is digitally processed so as to derive and record therefrom electronic data representing the magnitude of applied fluid pressure, and so as also to derive the length of time that positive fluid pressure is applied and the electronic data representing this information is automatically displayed and recorded. The controller is also programmable to permit optional selection and input of various control parameters, such as a maximum positive inflation pressure that is to be applied, maximum duration for applying positive inflation pressure, initialization of the date and time of an inflation procedure and/or retrieving and displaying inflation data previously recorded for any prior inflation of the balloon catheter or other balloon member.

System and method for monitoring and displaying balloon catheter

An electronically controlled syringe system for connection to a balloon catheter or other balloon-type member and for automatically monitoring, displaying and recording inflation data when the syringe system is used to inflate the balloon catheter or other balloon-type member. A syringe having a barrel and a syringe plunger is selectively operable to increase fluid pressure applied to the balloon catheter or other balloon member by sliding the plunger further into the barrel. Positive pressure applied to the balloon catheter or member can be released by withdrawing the syringe plunger toward the rear of the barrel. A piezoresistive semiconductor transducer housed on the barrel of the syringe senses positive fluid pressure applied by the syringe. The electric signal output by the transducer is input to a controller where the signal is digitally processed so as to derive and record therefrom electronic data representing the magnitude or applied fluid pressure, and so as also to derive the length of time that positive fluid pressure is applied and the electronic data representing this information is automatically displayed and recorded. The controller is also programmable to permit optional selection and input of various control parameters, such as a maximum positive inflation pressure that is to be applied, maximum duration for applying positive inflation pressure, initialization of the date and time of an inflation procedure and/or retrieving and displaying inflation data previously recorded for any prior inflation of the balloon catheter or other balloon member.

System and method for monitoring, displaying and recording balloon

A syringe and method for use which may be selectively operated between a free position and a locked position. A triggering device configured with a trigger attached to the plunger of the syringe is employed. The triggering device includes a set of threads located on the plunger and a corresponding set of threads on the barrel of the syringe. Upon actuation of the trigger, the threads on the plunger are retracted from their position of engagement with the threads on the barrel, thereby placing the syringe in position for free movement of the plunger with respect to the barrel. The threads are biased in the engaged position. Thus, when the trigger is released, the threads on the plunger return to their position of engagement with the threads on the barrel. In the locked position, the plunger may be screwed into or out of the barrel by rotating the plunger, enabling the operator of the syringe to maintain strict control over the amount of pressure in the syringe. The triggering device employs a plurality of ramp and channel configurations which are disposed at approximately the same angle as the threads on the plunger and barrel. Thus, upon actuation of the triggering device, no net force results on the plunger which would cause movement of the plunger with respect to the barrel.

Growing community of inventors

Salt Lake City, UT, United States of America

Darla R Gill