One or more oral devices having interdental anchors configured to elastically deform and engage with an interdental gap between adjacent teeth. One or more medical devices can then be secured to the oral device via a securing portion, allowing the medical device to be secured relative to the patient.

Disclosed herein are aspects of a tracheal breathing tube that provides for accurate and reliable control of cannula cuff pressure. Such a tracheal breathing tube include a pressure controller through which a fluid is supplied to a cannula cuff of a tracheal breathing tube and which enables reliable indication of a level of pressure of fluid within the cannula cuff. The pressure controller serves to achieve a proper interface between the cannula cuff and a patient's trachea, thereby addressing important clinical considerations such as anesthesiologist control. Moreover, the pressure controller serves to ensure that proper force is being applied on the patient's tracheal walls by the cannula cuff to thereby limit the potential for post-surgical complications resulting from, for example, inadequate blood supply to an organ or part of the body. swelling of the patient's tracheal walls that can lead to difficulty in breathing, and the like.

The present disclosure provides generally for a therapeutic oral device for sleep apnea and associated methods for using the device. According to the present disclosure, the device may comprise a hard palate portion, mouth guard portion, and a tongue retainer portion. The hard palate portion may comprise one or more materials. The hard palate portion may also comprise a composite of materials, including but not limited to embedded materials. The mouth guard portion may comprise one or more components that provide stability and maintain the position of the therapeutic oral device within the mouth. The tongue retainer portion may comprise an airway and a predetermined length. A method of use may comprise the utilization of one or more incremental oral devices to overcome a gag reflex. When the oral device is formed from a mold, the mouth guard portion and the hard palate portion may be custom fit to the dimensions of the intended mouth.

Various embodiments of a tracheostomy tube having neck flanges with filleted ends are provided. In certain embodiments, the neck flange may include a fillet extending from a bottom surface of the neck flange to a tip of the neck flange. In addition, the filleted end may also be tapered from a top surface of the neck flange to the tip of the neck flange. The neck flange may also include several curved edges, such as curved edges from the tip of the neck flange to side surfaces of the neck flange, and a curved bottom surface from side surface to side surface of the neck flange.

The improvement device provides an oral suction system for use with endo-tracheal tubes. The device provides alternative anti-infective components and a removable and/or disposable external sleeve, both for mitigation or elimination of risks for viral and/or bacterial contamination of the patient and healthcare professional.

A device and method for performing a cricothyrotomy and/or a tracheotomy has an outer cannula. An inner cutting cannula is positioned within the outer cannula. An actuator is coupled to a proximate end of the inner cutting cannula. The actuator keeps the inner cutting cannula in a retracted position within the outer cannula when the actuator is not activated and an extended position where a distal end of the inner cutting cannula extends out of the outer cannula with a force for the distal end of the inner cutting cannula to penetrate one of a cricothyroid membrane or tracheal wall when the actuator is activated.

The present invention provides medical devices comprising at least one visualization device sealed to, attached to or otherwise combined with at least one of the following second devices: an oral airway, ventilating mask, urinary catheter, trocar, a tool tube, and a medical glove. The present invention also provides methods for rapid and accurate placement of a medical device in a patient and continuous real time monitoring, including a remote monitoring, of the patient after the placement.

An airway holder for use in holding an airway device, such as an air or nose tube, has a first pair of wings symmetrically disposed about a center portion and a second pair of wings asymmetrically disposed about the center portion. One of the wings of the second pair of wings has an offset to facilitate that wing wrapping about a portion of the other wing of that pair about the airway device, before then, preferably being adhered to the face of the patient. The airway holder may be provided as a portion of a kit with eye protectors in an effort to remove surgical tape (and subsequent reuse with other procedures to potentially spread contamination).

A patient tube securement apparatus is disclosed that may be used for oral or nasal intubation of a patient.

The apparatus may comprise an endotracheal tube securement apparatus for securing an endotracheal tube to a patient, the apparatus comprising a dermal patch arranged to be positioned on the skin of the patient, and at least one tube holder on the dermal patch.

The apparatus may comprise a patient tube securement apparatus for securing a patient tube to a patient, the apparatus comprising a dermal patch arranged to be positioned on the skin of the patient, and at least one tube holder on the dermal patch.

Examples are provided in which the tube holder is adjustably mounted on the dermal patch such that the position of the tube holder on the dermal patch can be adjusted without removing the dermal patch from the skin of the patient.

A tracheal device for the assisted respiration of a patient includes a first tube having a proximal end to be arranged protruding from the mouth of the patient and connectable to a device for assisted respiration, a distal end adapted to cover an orifice, and a first sealing element coupled externally to the first tube. The tracheal device also includes a second tube having a distal end adapted to cover the orifice, a second sealing element coupled externally to the second tube, and a flexible and collapsible service duct stably coupled to the first tube and the second tube to allow the service duct and the first and the second tubes to be arranged in two configurations.