Abstract: The present disclosure provides a balloon dilation catheter that includes a handle, a substantially rigid inner guide member coupled to the handle, a shaft arranged over the inner guide member, a balloon coupled to the inner guide member, and a polymer ball tip 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.

Abstract: 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.

Abstract: A balloon dilation device includes a handle (110) that defines an internal cavity (116), a shaft (118) extending distally from the distal end of the handle, an inflatable balloon (126) disposed about the distal end of the shaft, and an inflation lumen (142) extending from an inflation port (144) of the handle to the inflatable balloon. The inflatable balloon is configured to be actuated between a contracted state and an expanded state. The shaft includes a vent lumen extending between a first opening at a distal end of the shaft and a second opening of the shaft is disposed in the internal cavity of the handle. A vent lumen of the shaft and a vent opening (158) in an exterior surface of the handle define an airflow pathway between the first opening and the vent opening.

Abstract: A pressure sensor configured for biological pressure measurement at a distal end portion of an elongated member comprises a dissolvable hydrophilic material coated on a surface of the pressure sensor. A guide wire for biological pressure measurement may include a tube extending along a longitudinal axis of the guide wire; and a pressure sensor for biological pressure measurement, at least a portion of the pressure sensor being mounted within the tube. The pressure sensor comprises a pressure sensor membrane facing a top side of the tube. A circumferential wall of the tube includes at least six openings: a first distal opening, a second distal opening located on a right side of the tube, a third distal opening located on a left side of the tube, a first proximal opening, a second proximal opening located on a right side of the tube, and a third proximal opening located on a left side of the tube.

Abstract: A method for preparing a sensor wire includes: providing a sensor wire configured for biological pressure measurement and including: an elongated member; and a pressure sensor configured for biological pressure measurement, the pressure sensor being mounted at a distal end portion of the elongated member, wherein a dissolvable hydrophilic material is coated on a surface of the pressure sensor; and submerging the pressure sensor in saline solution, whereby the hydrophilic material dissolves and causes the saline solution to contact the pressure sensor.

Abstract: 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.

Abstract: A pressure sensor configured for biological pressure measurement at a distal end portion of an elongated member comprises a dissolvable hydrophilic material coated on a surface of the pressure sensor. A guide wire for biological pressure measurement may include a tube extending along a longitudinal axis of the guide wire; and a pressure sensor for biological pressure measurement, at least a portion of the pressure sensor being mounted within the tube. The pressure sensor comprises a pressure sensor membrane facing a top side of the tube. A circumferential wall of the tube includes at least six openings: a first distal opening, a second distal opening located on a right side of the tube, a third distal opening located on a left side of the tube, a first proximal opening, a second proximal opening located on a right side of the tube, and a third proximal opening located on a left side of the tube.

Abstract: A guide wire for biological pressure measurement includes a tube extending along a longitudinal axis of the guide wire; and a pressure sensor for biological pressure measurement, at least a portion of the pressure sensor being mounted within the tube. The pressure sensor comprises a pressure sensor membrane facing a top side of the tube. A circumferential wall of the tube includes at least six openings: a first distal opening, a second distal opening located on a right side of the tube, a third distal opening located on a left side of the tube, a first proximal opening, a second proximal opening located on a right side of the tube, and a third proximal opening located on a left side of the tube. The first distal opening is larger than the second and third distal openings, and the first proximal opening is larger than the second and third proximal openings.

Abstract: The present disclosure provides a medical device (10) comprising a friction member (30, 48) configured to assist in controlling and/or limiting unintentional and/or undesirable movement between two releasably secured components (18, 28) of the medical device. The releasably secured components may be part of a resistance assembly for holding a medical device actuator (20) in a particular position and/or to improve the ease of which the activator moves into one position versus another position.

Abstract: The present disclosure provides a medical device (10) comprising a friction member (30, 48) configured to assist in controlling and/or limiting unintentional and/or undesirable movement between two releasably secured components (18, 28) of the medical device. The releasably secured components may be part of a resistance assembly for holding a medical device actuator (20) in a particular position and/or to improve the ease of which the activator moves into one position versus another position.

Abstract: A guide wire for biological pressure measurement includes a tube extending along a longitudinal axis of the guide wire; and a pressure sensor for biological pressure measurement, at least a portion of the pressure sensor being mounted within the tube. The pressure sensor comprises a pressure sensor membrane facing a top side of the tube. A circumferential wall of the tube includes at least six openings: a first distal opening, a second distal opening located on a right side of the tube, a third distal opening located on a left side of the tube, a first proximal opening, a second proximal opening located on a right side of the tube, and a third proximal opening located on a left side of the tube. The first distal opening is larger than the second and third distal openings, and the first proximal opening is larger than the second and third proximal openings.