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Clerc, MA

Claude Clerc, Marlborough, MA US

Patent application numberDescriptionPublished
20080221670RADIOPAQUE POLYMERIC STENT - The invention relates to an implantable radiopaque stent adapted to be disposed in a body lumen. In one aspect of the invention, at least one radiopaque filament is arranged for permanent attachment to a hollow tubular structure. The filament is desirably arranged in a linear direction traverse to a longitudinal length of the structure, the structure having a tubular wall that defines an inner surface and an outer surface and opposing first open end and second open end. The radiopaque filament improves external imaging of the tubular structure on fluoroscope or x-ray imaging equipment.09-11-2008
20080300673RADIOPAQUE COMPOSITIONS, STENTS AND METHODS OF PREPARATION - The invention relates to an implantable radiopaque stent adapted to be disposed in a body lumen. In one aspect of the invention, a plurality of elongate filaments including one or more radiopaque filaments are arranged to form a hollow tubular structure having a tubular wall that defines an inner surface and an outer surface and opposing first open end and second open end. One of the open ends of the stent is formed by an intersection of adjacent filament ends. A radiopaque compound is applied to the intersection, the radiopaque compound comprising radiopaque material and polymeric material. The radiopaque compound and radiopaque filament provide improved external imaging of the tubular structure on imaging equipment.12-04-2008
20090076526Compression, Banding and Percutaneous Airway Ligation of Emphysematous Lung Tissue - A lung volume reduction system includes a percutaneously, laparoscopically or thorocospically insertable delivery element comprising a control end which remains outside the body and an insertion end which, when in an operative position, is adjacent to an external surface of a target portion of a lung and a constriction element deployable from the distal end of the delivery element to apply compressive force to an external surface of the target portion of the lung to constrict at least one airway therein and collapse the target portion of the lung.03-19-2009
20090187240STENT WITH ANTI-MIGRATION FEATURE - An intraluminal prosthesis includes an outer three-dimensional (3D) anti-migration structure that is attached to the outer wall of a fully covered or partially covered stent to prevent migration and still allow stent removal at a later period of time. A method of manufacturing the intraluminal prosthesis includes attaching the anti-migration structure by usage of a polymer such as polyurethane.07-23-2009
20100057109ENDOSCOPIC SUTURING DEVICE - A suturing device for use in endoscopic procedures includes a head configured to be removably coupled to an elongate medical device and an actuator coupled to the head via an elongate flexible sheath. The suturing device is configured to pass a needle and suture through a selected tissue site upon actuation of the actuator. In another embodiment, a suturing device includes a head and a retaining portion configured to receive a guide wire. The suturing device can be inserted into a patient's body using the guide wire to guide and help position the head of the suturing device. In such an embodiment, the suturing device can also include an expandable member coupled to the head and that is configured to be expanded within a body lumen of a patient to help maintain a position of the head within the body lumen.03-04-2010
20100331960ENDOPROSTHESIS AND ENDOPROSTHESIS DELIVERY SYSTEM AND METHOD - An endoprosthesis includes a structure which is self-expandable from a reduced profile to an expanded profile. The structure has one or more longitudinal portions and a transverse central plane about which the one or more longitudinal portions are symmetric. A removable sheath retains the one or more longitudinal portions in the reduced profile. A release structure is coupled to the sheath for removal thereof from the one or more longitudinal portions to provide the self-expansion thereof to the expanded profile. A method for implanting the endoprosthesis into a body of a patient includes inserting the structure which is covered by the sheath into the body of the patient such that the structure has the reduced profile. The release structure is then actuated for removing the sheath from the one or more longitudinal portions to provide the self-expansion to the expanded profile.12-30-2010
20110251525SYSTEMS AND METHODS FOR TREATING LUNG TISSUE - A system for treating lung tissue includes a tube having a distal end, an anchoring device secured to the tube, the anchoring device configured to anchor at least a portion of the tube against an esophagus, a trachea, or a bronchus; and an ablation device carried within a lumen of the tube.10-13-2011
20110265908APPARATUS AND METHOD FOR MANUFACTURING A SINGLE WIRE STENT - A mandrel for manufacturing a stent from a single wire includes a cylindrical member having a plurality of pins at a proximal end region, a plurality of pins at a distal end region, and a plurality of indentations between the proximal pins and the distal pins. These indentations form a helical pattern on the outer surface of the cylindrical member. The single wire is wrapped around every proximal pin and distal pin on the mandrel by following the indentations in the mandrel. The single wire is slid through the indentation under any crossing section of wire and over the next crossing section of wire in an under-over pattern.11-03-2011

Patent applications by Claude Clerc, Marlborough, MA US

Claude Clerc, Marlboro, MA US

Patent application numberDescriptionPublished
20110172585ANTI-OBESITY DUAL STENT - The anti-obesity dual stent includes a tubular outer structure within which is located a coaxial tubular inner structure. The outer structure is sized to fit within a duodenum in substantially coaxial relation therewith. The outer and inner structures communicate with the pylorus and papilla of Vater to provide conduits for the chyme and digestive fluid. Alternatively, the anti-obesity dual stent may include a tubular papilla-supplied structure which has a lateral orientation relative to a tubular pylorus-supplied structure. The papilla-supplied and pylorus-supplied structures each are sized to fit longitudinally within the duodenum. The pylorus-supplied and papilla-supplied structures communicate with the pylorus and papilla of Vater to provide conduits for the chyme and digestive fluid.07-14-2011
20110270406Anti-Obesity Stent - The anti-obesity stent includes a tubular structure having outer and inner surfaces and proximal and distal ends. The tubular structure is sized to fit within a duodenum in substantially coaxial relation therewith. The tubular structure is impervious or semi-permeable to digestive substances and chyme within the duodenum. The anti-obesity stent includes a transport structure at least a part of which is coincident with or connected to the outer surface. The transport structure extends to the distal end of the tubular structure. At least one retainer structure is connected to the tubular structure. The retainer structure secures the tubular structure within the duodenum such that the transport structure is positioned to receive digestive fluids from a papilla of Vater on an inner surface of the duodenum. The transport structure provides a conduit for the digestive fluids therein to flow to the distal end.11-03-2011

Claude Clerc, Malborough, MA US

Patent application numberDescriptionPublished
20110270405Duodenal Metabolic Stent - In at least one embodiment, the invention is directed to an endoluminal device comprising a stent and a sleeve. In one embodiment, the endoluminal device is implanted in a portion of the gastrointestinal tract. In some embodiments, the stent has a first region and a second region where the first and second regions provide different levels of radial force. In one embodiment, the first region is made from a plurality of first wires having a first diameter and the second region is made from a plurality of second wires having a second diameter which is smaller than the first diameter. In other embodiments, the endoluminal device has at least one engagement mechanism engaging the stent to the sleeve, the endoluminal device to a body lumen, and any combination thereof. In at least one embodiment, the endoluminal device has a wall with at least one opening therein.11-03-2011

Claude O. Clerc, Marlborough, MA US

Patent application numberDescriptionPublished
20090054972ATRAUMATIC STENT WITH REDUCED DEPLOYMENT FORCE, METHOD FOR MAKING THE SAME AND METHOD AND APPARATUS FOR DEPLOYING AND POSITIONING THE STENT - An implantable stent includes a plurality of elongate wires braided to form a hollow tubular structure having a tubular wall to define an interior surface and an exterior surface and having opposed open first and second ends, wherein the opposed open first and second ends are atraumatic ends The atraumatic ends of the stent are desirably free of any loose wire ends. The wires include composite wires to enhance visibility of the wires to provide improved external imaging of the wires in the body. The elongate composite wires of the stent may be metallic wires having an outer metallic portion including a first metal, such as nitinol, and an inner metallic core portion including a second metal, which is a radiopaque material, such as gold, barium sulfate, ferritic particles, platinum, platinum-tungsten, palladium, platinum-iridium, rhodium, tantalum or combinations thereof.02-26-2009
20090082840METHOD FOR LOADING A STENT INTO A DELIVERY SYSTEM - Methods for assembling a stent delivery system are provided, as well as the stent delivery assemblies and devices formed by such methods. Also provided is a method for loading a stent into a delivery system.03-26-2009
20090220677METHOD OF MANUFACTURING A COVERED STENT - A method of manufacturing a covered stent having a sufficiently thick covering to retain a therapeutically effective amount of a therapeutic agent. The covering is applied to the entire outer surface of the stent to provide sufficient volume for retention of the therapeutic agent. In certain embodiments, the stent has a plurality of openings that are covered by the covering. The invention is particularly suited for certain applications, such as for the manufacture of non-vascular stents.09-03-2009
20100100170SHAPE MEMORY TUBULAR STENT WITH GROOVES - An implantable, radially distensible stent includes a tubular structure having opposed open ends. The wall of the stent is made from a shape memory polymeric material. Grooves may be disposed within an outer surface of stent wall to improve flexibility and drainage of the stent.04-22-2010
20110079315ATRAUMATIC STENT WITH REDUCED DEPLOYMENT FORCE, METHOD FOR MAKING THE SAME AND METHOD AND APPARATUS FOR DEPLOYING AND POSITIONING THE STENT - An implantable stent includes a plurality of elongate wires braided to form a hollow tubular structure having a tubular wall to define an interior surface and an exterior surface and having opposed open first and second ends, wherein the opposed open first and second ends are atraumatic ends. The atraumatic ends of the stent are desirably free of any loose wire ends. The wires include composite wires to enhance visibility of the wires to provide improved external imaging of the wires in the body. The elongate composite wires of the stent may be metallic wires having an outer metallic portion including a first metal, such as nitinol, and an inner metallic core portion including a second metal, which is a radiopaque material, such as gold, barium sulfate, ferritic particles, platinum, platinum-tungsten, palladium, platinum-iridium, rhodium, tantalum or combinations thereof.04-07-2011

Patent applications by Claude O. Clerc, Marlborough, MA US

Matthew R. Clerc, Acushnet, MA US

Patent application numberDescriptionPublished
20100071228ARTICLES OF FOOTWEAR - An article of footwear includes a footwear upper and a sole assembly secured to the footwear upper. The sole assembly has a heelward portion and a toeward portion, and includes a deck assembly disposed substantially in the heelward portion of the sole assembly. The deck assembly includes an upper deck portion, a lower deck portion spaced from the upper deck portion, and right and left supports attached to respective right and left portions of the upper and lower deck portions substantially near respective right and left lateral edges of the upper and lower deck portions. The deck assembly defines a cavity between the upper and lower decks. The deck assembly directs translation of ground contact forces incurred by the heelward portion of the sole assembly at least partially laterally outwardly.03-25-2010
20100126043Articles of Footwear - An article of footwear promotes complimentary movement and proprioceptive feedback of a user's foot (e.g., to help an infant learn to walk or an adult balance on an uneven surface) while wearing the article of footwear. The article of footwear includes an outsole having a forefoot region, a heel region, and a mid region substantially in between the forefoot and heel regions. The three regions are configured to provide complimentary movement with respect to the user's foot. The forefoot region of the outsole includes a base portion interconnecting ground contact pads configured to move relative to one another, each ground contact pad moving substantially independently of the other relative to the base portion.05-27-2010