Abstract: An implantable delivery device and method for utilizing the device to delivery a bioactive agent to a subject in need thereof is described. The device includes a pattern of structures fabricated on a surface of the device to form a nanotopography. A random or non-random pattern of structures may be fabricated such as a complex pattern including structures of differing sizes and/or shapes. The device may be located adjacent tissue such as an endovascular implant or a perivascular implant, and may deliver the bioactive agent without triggering an immune or foreign body response to the bioactive agent.

Abstract: An implantable delivery device and method for utilizing the device to delivery a bioactive agent to a subject in need thereof is described. The device includes a pattern of structures fabricated on a surface of the device to form a nanotopography. A random or non-random pattern of structures may be fabricated such as a complex pattern including structures of differing sizes and/or shapes. The device may be located adjacent tissue such as an endovascular implant or a perivascular implant, and may deliver the bioactive agent without triggering an immune or foreign body response to the bioactive agent.

Abstract: An implantable delivery device and method for utilizing the device to delivery a bioactive agent to a subject in need thereof is described. The device includes a pattern of structures fabricated on a surface of the device to form a nanotopography. A random or non-random pattern of structures may be fabricated such as a complex pattern including structures of differing sizes and/or shapes. The device may be located adjacent tissue such as an endovascular implant or a perivascular implant, and may deliver the bioactive agent without triggering an immune or foreign body response to the bioactive agent.

Abstract: A stoma dilation device that includes a tubular support defining a continuous pathway through the device; an inflatable dilation balloon located on the tubular support, the inflatable dilation balloon including a dilation region forming a first portion of the device and a retention region forming a second portion of the device; and a balloon inflation lumen. The retention region of the balloon is configured to have a diameter upon full, unrestrained inflation that is greater than the diameter of the dilation region.

Abstract: The present disclosure is directed to a medical port drainage assembly that includes a port component and a replaceable catheter. The port component includes a tube having a proximal end, a distal end, and tube walls defining a catheter access lumen. A head component is located on a proximal end of the tube and an assembly retention element is located on a distal end of the tube. The head component is deployed outside the patient's body and defines an opening to the catheter access lumen. The assembly retention element is deployed within a lumen of the patient's body. The port component includes a valve assembly which may be a single valve (e.g., a duckbill valve) or a system of valves. The port component also includes a connector for coupling and decoupling the replaceable catheter to the port component.

Abstract: A stoma dilation device that includes a tubular support defining a continuous pathway through the device; an inflatable dilation balloon located on the tubular support, the inflatable dilation balloon including a dilation region forming a first portion of the device and a retention region forming a second portion of the device; and a balloon inflation lumen. The retention region of the balloon is configured to have a diameter upon full, unrestrained inflation that is greater than the diameter of the dilation region.

Abstract: A stoma dilation device that includes a tubular support defining a continuous pathway through the device; at least one inflatable dilation balloon and at least one inflatable retention balloon located on the tubular support; and inflation lumens for each balloon. The inflatable dilation balloon forms at least a first portion of the device and the inflatable retention balloon forms at least a second portion of the device. The inflatable retention balloon is configured to have a diameter upon full, unrestrained inflation that is greater than the largest diameter of the inflatable dilation balloon upon inflation.

Abstract: There is provided an enteral feeding assembly having a base and a connector. The base has a catheter with a lumen for communication with a body lumen. The base also has an opening with a predetermined shape on its proximal side that also communicates with the catheter lumen. The connector has a key configured to complement the predetermined shape of the opening in the base, which occurs desirably in one position only, so that the connector and base may be joined together. The connector is also connected to a feeding tube that provides a nutrient solution from a replaceable feeding bag. Once the connector is in position in the base, liquid may from the bag to the body lumen. Once in position, the connector may rotate 360 degrees relative to the base before being again in the installation/removal position.

Abstract: A configurable percutaneous endoscopic gastrostomy tube includes a shaft having a distal end and a proximal end. The shaft defines a lumen therethrough for passage of a feeding solution or medicine. An expandable retainer is located on the shaft, the retainer having a deployed position and an insertion position. The tube includes a releasable lock for maintaining the expandable retainer in its deployed position, the releasable lock located on the shaft proximal to the expandable retainer. A flexible sheath surrounds the expandable retainer, the sheath being generally loose around the retainer when the retainer is in an insertion position and the sheath being generally snug against an exterior surface of the retainer when the retainer is in a deployed position.

Abstract: The present disclosure describes a single incision method of placing a drainage catheter in the peritoneal cavity.

Abstract: An implantable delivery device and method for utilizing the device to delivery a bioactive agent to a subject in need thereof is described. The device includes a pattern of structures fabricated on a surface of the device to form a nanotopography. A random or non-random pattern of structures may be fabricated such as a complex pattern including structures of differing sizes and/or shapes. The device may be located adjacent tissue such as an endovascular implant or a perivascular implant, and may deliver the bioactive agent without triggering an immune or foreign body response to the bioactive agent.

Abstract: The present disclosure describes a cecostomy tube having a head with an opening and a valve. There is a flexible catheter with a lumen having proximal and distal ends, the proximal end of the catheter in fluid communication with the opening in the head, a portion of the catheter extending away from the head to define the distal end. The catheter also has walls defining inside and outside surfaces from the opening defined in the head to the distal end of the catheter. There is a retainer provided on the distal end of the catheter. The retainer can change shape from a first profile or configuration to a second profile where the second profile is larger than the first profile and the second profile is adapted to retain the cecostomy tube in place in a body. The device may be placed in a single, initial surgical operation.

Abstract: There is provided a drainage catheter system. The system includes an elongated tube having a substantially consistent cross-sectional size between a proximal end and a distal end. The tube has side walls defining a drainage lumen and the distal end of the tube is desirably closed. The tube further includes a plurality of holes in at least a portion of the side wall of the tube. These holes are provided along a length of the tube to define a drainage section of the catheter. The tube may include a hydrophilic coating on at least a portion of the exterior of the tube. The distal end of the tube may be tapered. The system also includes a head which is deployed outside the human body. The head is located on a proximal end of the tube and includes an opening to the drainage lumen of the tube.

Abstract: There is provided a suction catheter having a tubular body with a lumen formed therethrough. The catheter has a plurality of spaced elongated apertures positioned near its distal tip. The catheter may have a fourth round opening positioned proximally to the three openings. The catheter has reduced impact force compared to similar suction catheters without the plurality of apertures near the distal tip.

Abstract: The present disclosure describes an adapter for use with two connectors in, for example, a pleural, peritoneal or other bodily fluid drainage system. The adapter allows the use of the disposal bag from one manufacturer to be used with the catheter of another. This simplifies the storage requirements of distributors and hospitals and reduces the everyday challenges faced by those patients requiring fluid drainage.

Abstract: The present disclosure describes a cecostomy tube having a head with an opening and a valve. There is a flexible catheter with a lumen having proximal and distal ends, the proximal end of the catheter in fluid communication with the opening in the head, a portion of the catheter extending away from the head to define the distal end. The catheter also has walls defining inside and outside surfaces from the opening defined in the head to the distal end of the catheter. There is a retainer provided on the distal end of the catheter. The retainer can change shape from a first profile or configuration to a second profile where the second profile is larger than the first profile and the second profile is adapted to retain the cecostomy tube in place in a body. The device may be placed in a single, initial surgical operation.

Abstract: A container for sterilizing and storing surgical materials and preserving surgical materials in a sterilized condition is disclosed herein. The container includes a lid, liner and in many embodiments, a frame. The lid and liner are desirably disposable and recyclable after a single use while the frame should be reusable many times. The liner and optionally the lid is substantially transparent so that a user can inspect the instruments while the container is closed without compromising the sterile nature of the inside of the container.

Abstract: A stoma dilation device that includes a tubular support defining a continuous pathway through the device; an inflatable dilation balloon located on the tubular support, the inflatable dilation balloon including a dilation region forming a first portion of the device and a retention region forming a second portion of the device; and a balloon inflation lumen. The retention region of the balloon is configured to have a diameter upon full, unrestrained inflation that is greater than the diameter of the dilation region.

Abstract: A configurable percutaneous endoscopic gastrostomy tube includes a shaft having a distal end and a proximal end. The shaft defines a lumen therethrough for passage of a feeding solution or medicine. An expandable retainer is located on the shaft, the retainer having a deployed position and an insertion position. The tube includes a releasable lock for maintaining the expandable retainer in its deployed position, the releasable lock located on the shaft proximal to the expandable retainer. A flexible sheath surrounds the expandable retainer, the sheath being generally loose around the retainer when the retainer is in an insertion position and the sheath being generally snug against an exterior surface of the retainer when the retainer is in a deployed position.

Abstract: A stoma dilation device that includes a tubular support defining a continuous pathway through the device; at least one inflatable dilation balloon and at least one inflatable retention balloon located on the tubular support; and inflation lumens for each balloon. The inflatable dilation balloon forms at least a first portion of the device and the inflatable retention balloon forms at least a second portion of the device. The inflatable retention balloon is configured to have a diameter upon full, unrestrained inflation that is greater than the largest diameter of the inflatable dilation balloon upon inflation.