An oropharyngeal airway for use during diagnostic and surgical procedures, comprising a body with a proximal and a distal end. The distal end is sized for insertion through a protective bite block disposed in a patient's mouth. Both sides of the distal end are tapered to a curved distal edge. A flange is transversely opposed at the proximal end, preventing the proximal end from moving through the protective bite block and into the patient's mouth. An elliptically-arched channel in the shape of a lingual contour extends from the proximal end to the distal end. The channel includes a pair of tapered upstanding walls that guide the passage of a surgical instrument through the space between them. The oropharyngeal airway can be constructed of recyclable or biodegradable materials and is compatible with protective bite blocks of all sizes.

A device is disclosed to assist in making a customized intraoral positioning device IPD to be positioned within a mouth of a patient in accordance with a prescribed radiation therapy treatment plan for a head and/or neck of the patient, the prescribed radiation therapy treatment plan including an incisor separation and/or tongue position of the patient, the device comprising: a base unit configured to be positioned between upper and lower arches in the patient's mouth, wherein the base unit includes an arch section for incisor separation in a deployed configuration in the patient's mouth and first and second arms that extending from the arch unit; a handle extending from the base unit to enable a user to grasp the device so that the user may introduce and remove the device from the patient's mouth; and one or more bite blocks configured on the arch section of the base unit so as to increase the height of the arch section in accordance with the incisor separation of the prescribed radiation therapy treatment plan, to thereby enable a user to obtain records of the position for dental and oral structure within the patient's mouth including a relationship between the upper and lower arches at the prescribed incisor separation.

A method is disclosed of making a customized intraoral positioning device to be positioned within a patient's mouth for radiation therapy planning and treatment of a head and/or neck of the patient.

A method is disclosed of making a customized intraoral positioning device to be positioned within a patient's mouth for radiation therapy planning and treatment of a head and/or neck of the patient.

Illuminated dental instrument assemblies (e.g., illuminated dental mirrors, illuminated dental wedges, trans-illumination dental instrument, illuminated dental bite blocks, etc.) are provided. The illuminated dental instrument assemblies may be adapted to be periodically sterilized. The illuminated dental instrument assemblies may include a magnetically energetic fiber optic coupler. The magnetically energetic fiber optic coupler may be configured to allow the illuminated dental instrument assembly to rotate with respect to an associated fiber optic cable that is removably connected to the magnetically energetic fiber optic coupler. The illuminated dental instrument assemblies may include a fiber optic material that is encapsulated.

Illuminated dental instrument assemblies (e.g., illuminated dental mirrors, illuminated dental wedges, trans-illumination dental instrument, illuminated dental bite blocks, etc.) are provided. The illuminated dental instrument assemblies may be adapted to be periodically sterilized. The illuminated dental instrument assemblies may include a magnetically energetic fiber optic coupler. The magnetically energetic fiber optic coupler may be configured to allow the illuminated dental instrument assembly to rotate with respect to an associated fiber optic cable that is removably connected to the magnetically energetic fiber optic coupler. The illuminated dental instrument assemblies may include a fiber optic material that is encapsulated.

The present disclosure is directed to a forceps having an end effector assembly including first and second jaw members. At least one of the jaw members is movable relative to the other between a spaced-apart position and an approximated position for grasping tissue therebetween. Each jaw member includes an electrically-conductive tissue-contacting surface adapted to connect to a source of energy to treat tissue grasped between the jaw members. A suction system is disposed proximate the first and second jaw members and is configured to apply suction to a surgical site upon activation thereof.

A catheter with three distinct compression resistance coils, including a body coil and two pull wire coils, is disclosed. The triple coil system can provide maximal resistance to compression of the catheter's proximal shaft, as well as maximization of the curve angle that the catheter tip can achieve. Additionally, the tri-coil catheter can allow for a lower initial compression load and a more flexible proximal shaft. A gap between the outer diameter of the pull wire and the inner diameter of the pull wire compression coil that is equal to about 10-30% of inner diameter of the pull wire compression coil can provide optimal catheter performance.

The retractor is a generally U-shaped device for protecting the cheek and tongue from instruments used during dental and prosthodontic procedures. The retractor has a planar base defined by two spaced arms, a pair of upright shields extending from the arms, and a posterior connector connecting the shields. The base is contoured to grip the tooth adjacent to the tooth to be treated, and thereby, secure the retractor within the patient's mouth.

The retractor is a generally U-shaped device for protecting the cheek and tongue from instruments used during dental and prosthodontic procedures. The retractor has a planar base defined by two spaced arms, a pair of upright shields extending from the arms, and a posterior connector connecting the shields. The base is contoured to grip the tooth adjacent to the tooth to be treated, and thereby, secure the retractor within the patient's mouth.