Abstract: A bone fracture fixation system including reference pins inserted into bone fragments of a patient in a first configuration and an image capture device configured to capture an image of the reference pins, and the bone fragments. The system includes a processor configured to receive and pre-process the captured image data. The processor pre-processes the image data by virtually re-positioning the reference pins in the first configuration into a second configuration, wherein the re-positioning virtually re-positions the bone fragments into normal alignment; and virtually generating a support device. The system includes a point-of-care production apparatus that produces a three-dimensional model of the virtually generated support device in a form that can be applied to the patient.

Abstract: The present invention provides a spinal plate which is used to perform fixation surgery on a spine in orthopedic surgery and neurosurgery. The spinal plate comprises a central body and a pair of rotation portions which are disposed on both sides in a longitudinal direction of the central body and each of the pair of rotation portions has bone screw. The spinal plate also comprises spike screw in each of the pair of rotation portions. Each of the pair of rotation portions include a rotation connection portion, and the central body includes a rotation support portion. Rotation pins are used to connect the central body with the pair of rotation portions disposed on both sides in a longitudinal direction of the central body and enable the pair of rotation portions to rotate clockwise or counterclockwise with respect to the central body.

Abstract: The present invention discloses an interspinous process fusion device, a method of fabricating the interspinous process fusion device, and a surgical method for maintaining a space between two spinous processes in a spine of a patient using the fusion device. The interspinous process fusion device including a distal tip member, a middle plate, a proximal plate, an elongate member, and a plurality of movable wings. The elongate member having a first end, a second end, and a longitudinal axis extending between the first and second end. The distal tip member is connected to the first end of the elongate member, the proximal plate is connected to the second end of the elongate member, and the middle plate and plurality of wings are positioned intermediate the distal tip member and the proximal plate along the longitudinal axis to form the interspinous process fusion device assembly.

Abstract: A fixation system for repairing a pars fracture includes a needle guide configured to be docked on a lamina of the pars, a needle, a guidewire, and a screw assembly. A portion of the needle is configured for insertion through a passage of the needle guide. A portion of the guidewire is configured for insertion through a passage of the needle. The screw assembly includes a collar and an elongated portion, the collar being movable with respect to the elongated portion. A portion of the screw assembly is configured to contact the lamina co-axially with the guidewire.

Abstract: The disclosure provides example methods, systems and apparatus for stabilization of a rib. An example method includes: (a) accessing a medullary canal of a rib having a fracture, (b) advancing a guidewire into the medullary canal across the fracture, (c) advancing a delivery catheter containing a stent over the guidewire into the medullary canal and across the fracture, (d) retracting the delivery catheter relative to the stent, and (e) expanding the stent in the medullary canal.

Abstract: A wrist implant comprising a body section wherein the body section is elongated, wherein the body section has a first end and a distal end along the longitudinal extension of the body section with an elongated opening positioned adjacent to the first end in the body section, at least one wing section coupled to the body section and extending substantially transverse to the elongated extension of the body section, at least one opening in said elongated extension, and at least one opening positioned in the distal end of the body section.

Abstract: Implants, systems and methods for correcting bone deformities and fractures in the lower extremity are disclosed. Specifically, implants, systems and methods used for correcting bone deformities and/or fractures in the foot using compression are disclosed. A nail system including a first member with a first deformable member positioned at a first end of the first member and a second member received within the first member.

Abstract: An internal fixator apparatus comprises a barrel member having a bone interface adapted to be anchored to a first part of a bone in an extramedullary connection. A piston member has a bone interface adapted to be anchored to a first part of a bone, the piston member including a threaded nut portion, the barrel member and the piston member being operatively connected to concurrently form a joint whereby the barrel member and the piston member are displaceable at least in translation relative to one another. A fixator mechanism is inside the barrel member and the piston member, the fixator mechanism comprising at least a leadscrew threadingly engaged with the threaded nut portion, and at least one magnet connected to the leadscrew to rotate concurrently therewith, the magnet being rotatingly received in the barrel member.

Abstract: An embodiment of a body bead for a bone fracture fixation device, such as a rodscrew, includes at least one pocket and at least one tab. Each of the at least one pocket is configured to engage a respective one of at least one tab of an adjacent body bead and to withstand, without being significantly deformed, a torque of at least three N·m while rotating with the adjacent body bead. And each of the at least one tab is configured to engage a respective one of at least one pocket of another adjacent body bead and to withstand, without being significantly deformed, a torque of at least three N·m while rotating with the other adjacent body bead.

Abstract: A device including a first plate configured to interface with a first bone structure of a joint; a second plate configured to interface with a second bone structure of the joint opposite the first bone structure; and at least one mechanical actuation mechanism disposed between the first plate and the second plate and configured to apply a distraction force along an axis between the first plate and the second plate so as to urge the first plate and the second plate away from one another, wherein the device is configured so as to have a range of motion ranging from a minimum distance between the first plate and the second plate to a maximum distance between the first plate and the second plate, and wherein the mechanical actuation mechanism is configured such that the distraction force is substantially constant distraction force across the range of motion.

Abstract: The present disclosure relates to a thermal ablation probe device that integrates deployable sensors with a freezing probe or heating probe for use in ablating tissues. The ablation probe includes a longitudinal body including a thermal ablation energy source which may be, e.g., a cryosource or a heat source. The longitudinal body has a proximal end and a distal end terminating at a probe tip; and at least one deployable assembly disposed within the longitudinal body. The deployable assembly includes a flexible and substantially rigid deployment member, and at least one sensor affixed to a distal end of the deployment member. The ablation probe further includes a control mechanism for controlling deployment and retraction of the deployable assembly.

Abstract: An ablation applicator for an ablation device for ablating tissue of a blood vessel having a tubular body defining an inner lumen to which an ablation medium is conductible, a control mechanism for converting the tubular body between a passive operation mode for inserting the ablation applicator into the blood vessel and an active operation mode for ablating tissue of the blood vessel, and an ablation medium supply line for supplying the ablation medium to the inner lumen and positioned within the inner lumen and having a number of openings for passing the ablation medium from the ablation medium supply line to the inner lumen for thermally contacting the ablation medium with the tubular body wherein at least some of the openings are distributed along the ablation medium supply line with a predetermined spacing between neighboring openings.

Abstract: Devices, agents, and associated methods for selective modulation of renal nerves by localized delivery of neural ablative substances are disclosed herein. One aspect of the present technology is directed to a method for delivering a neuromodulatory agent (e.g., capsaicin) via a catheter to a kidney of the patient. The neuromodulatory agent selectively neuromodulates afferent renal nerves in a patient compared efferent renal nerves of the patient. The method can also include removing the catheter from the patient after delivering the neuromodulatory agent to conclude the procedure.

Abstract: An auxiliary return system for use with a bipolar electrosurgical device includes a tissue guard defining open proximal and distal ends and a body extending therebetween. The body includes outer and inner peripheral surfaces, the inner peripheral surface defining a lumen extending between the open proximal and distal ends, the outer peripheral surface including an elongated channel defined therein configured to receive a ground wire, a distal end of the elongated channel includes a pocket defined between the inner and outer peripheral surfaces of the body. An electrically conductive rivet includes a proximal end configured to engage the inner peripheral surface of the body and a distal end configured to engage the outer peripheral surface of the body to secure the rivet within the pocket. The distal end including a connector configured to engage the ground wire to provide electrical continuity between the ground wire and the rivet.

Abstract: An electrosurgical instrument is disclosed, having a first electrode having a planar face, a second electrode; an electrically insulative body, a fluid channel, a conductive wire, and a tubular seal. The tubular seal prevents saline from extending into a gap between the wire and the electrically insulative body of the instrument. The tubular seal is disposed around the wire, and extends between the wire and the body.

Abstract: A medical device includes an electrode shaft and a tip. The electrode shaft is configured to deliver energy to a target site and includes an electrode shaft lumen configured to deliver fluid to the target site. The tip is coupled to a distal tip of the electrode shaft. The tip includes an inner portion of conductive material and an exterior layer of insulative material. The tip includes a tip lumen fluidly connected to the electrode shaft lumen and configured to deliver fluid to the target site.

Abstract: An electrode assembly for an electrosurgical instrument includes a housing having an active electrical connector and a return electrical connector configured to operably engage a distal end of an electrosurgical instrument shaft, the housing encapsulating an elongated return electrode and a pair of insulative tubes configured to house a wire-like active electrode. The elongated return electrode includes a clevis at a distal end thereof and operably engages to the return electrical connector at a proximal end thereof. The wire-like active electrode operably engages at one end to the active electrical connector. A donut-like insulator is operably engaged to the clevis of the elongated return electrode and is configured to support the wire-like active electrode therearound. A tensioning mechanism is configured to operably engage an opposite end of the wire-like electrode and tension the wire-like active electrode about the donut-like insulator during assembly.

Abstract: The invention is within the general field of electroporation. In particular, the invention is within the general field of endoscopic electroporation and relates to a bipolar electrode suitable for endoscopic use, i.e. an electrode assembly that can be inserted in a resectoscope and deployed so as to treat e.g. internal organs tumors, such as bladder, rectum or esophagus.

Abstract: An irrigated electrophysiology catheter has a tip electrode having a shell, and a support member configured to plug the shell and support one or more tip components and/or facilitate their functions. Advantageously, the support member has an electrically-conductive interface portion and an insert-molded portion, wherein the interface portion, typically constructed of a precious metal alloy, is structurally minimized, yet still configured for electrical connection with the shell and the lead wire, so as to reduce the amount and hence the cost of its manufacture, whereas the insert-molded portion is constructed of a significantly less-costly material and is readily configured with micro-complex 3-D geometry adapted to support tip structure and functions including irrigation, force sensing and temperature sensing, as a further cost savings in the manufacturing of the tip electrode by reducing materials, labor and time.

Abstract: There is disclosed a method of treating affected external or surface tissue comprising the steps of providing a source of affected external or surface tissue; generating a source of microwave energy; transmitting said microwave energy into said affected external or surface tissues; exposing said affected external and surface tissues to said microwave energy to raise the local temperature to thereby ablate, remove, coagulate or otherwise alter said affected external and surface tissues.

Abstract: A system and method enabling the receipt of image data of a patient, identification of one or more locations within the image data depicting symptoms of COPD, analyzing airways and vasculature proximate the identified locations; planning a pathway to the one or more locations, navigating an extended working channel to one of the locations, positioning a microwave ablation catheter proximate the location, and energizing the microwave ablation catheter to treat the locations depicting symptoms of COPD.

Abstract: Devices and systems used to ablate tissue of a tumor using laser energy are disclosed. The devices and systems include a laser probe and a magnetic resonance (MR) safe temperature probe. The MR safe temperature probe includes an optical sensor. A bone anchor fixture separates the laser probe and the MR safe temperature probe to prevent interference in the MR safe temperature probe data. Proton Resonance Frequency (PRF) thermometry is used to model a temperature of a pixel of an MR image located adjacent the optical sensor. The modeled pixel temperature and the measured temperature are compared and monitored. Exceeding a threshold difference value causes an intervening action to occur.

Abstract: A catheter system (100) for placement within a treatment site (106) at a vessel wall (208A) or a heart valve includes an energy source (124), a balloon (104), an energy guide (122A), and a tissue identification system (142). The energy source (124) generates energy. The balloon (104) is positionable substantially adjacent to the treatment site (106). The balloon (104) has a balloon wall (130) that defines a balloon interior (146). The balloon (104) is configured to retain a balloon fluid (132) within the balloon interior (146). The energy guide (122A) is configured to receive energy from the energy source (124) and guide the energy into the balloon interior (146) so that plasma is formed in the balloon fluid (132) within the balloon interior (146). The tissue identification system (142) is configured to spectroscopically analyze tissue within the treatment site (106).

Abstract: A procedure is performed with respect to a skeletal portion within a body with a tool mounted upon a steerable arm. 3D image data is acquired of the skeletal portion. First and second x-ray images of the tool and the skeletal portion are acquired from respective first and second views. A computer processor (22) (i) registers the first and second images to the image data, (ii) identifies a location of the tool with respect to the skeletal portion, within the first and second images, (iii) determines the tool's location with respect to the image data, (iv) compares the tool's location with a designated locational element, (v) calculates the 3D difference between the tool's location and the locational element, and (vi) generates steering instructions for the arm such that the tool's location matches the locational element. Other applications are also described.

Abstract: Embodiments described herein provide various examples of mitigating electrical burn risks when using a monopolar electrosurgery tool on a patient in an electrosurgery procedure. In one aspect, a process receives an electrode configuration of the monopolar electrosurgery tool which includes a location of an active electrode of the monopolar electrosurgery tool at a surgical site on the patient's body and a location of a return electrode of the monopolar electrosurgery tool elsewhere on the patient's body. The process further obtains information of a metal implant inside the patient's body. Next, the process computes a plurality of potential current paths between the locations of the active electrode and the return electrode. The process then determines if one or more current paths in the plurality of computed potential current paths flow through the metal implant. If so, the process informs a surgical staff of potential electrical burn injuries associated with the electrode configuration.

Abstract: A marker for image guided surgery, consisting of a base, having a base axis, connecting to a clamp; and an alignment target. The alignment target includes a target region having an alignment pattern formed thereon, and a socket connected to the target region and configured to fit rotatably to the base, whereby the alignment target is rotatable about the base axis. The alignment target also includes an optical indicator for the socket indicating an angle of orientation of the alignment target about the base axis.

Abstract: A method includes providing medical images of a subject for selecting a target image from thereamong, building a 3D image model based on the medical images and the target image with a surgical target site assigned, performing image registration to superimpose the 3D image model on a real-time image of the subject so as to result in a combined image, determining a virtual entry site located on the combined image, connecting the surgical target site and the virtual entry site with a straight line, generating a guiding path extending from the virtual entry site, in a direction away from the surgical target site and along the straight line, and displaying the guiding path for guiding a surgical instrument.

Abstract: The present invention relates to a dental tool system, comprising a detection system (101) for detecting a spatial position (103-Z) of a tooth (115) or a tooth situation and a spatial tool position (103-W) of a tool (107); and a device (105) for controlling or regulating the tool (107) on the basis of the detected tool position (103-W) in relation to the position (103-Z) of the tooth (115) or the tooth situation.

Abstract: A magnetic tracking device is configured to track an object in an environment by receiving a measurement of the non-magnetic signal and a corresponding measurement of the magnetic signal for a location of the magnetic tracking device in the environment. The magnetic tracking device estimates, based on the measurement of the non-magnetic signal, a non-magnetic pose of the magnetic tracking device in the environment for the location. The device estimates, based on the measurement of the magnetic signal, a magnetic pose of the magnetic tracking device in the environment for the location. The device determines a difference between the magnetic pose estimate and the non-magnetic pose estimate for the location. The device determines a magnetic distortion correction value for the location based on the difference. The magnetic tracking device generates a distortion correction model including the distortion value and outputs a representation of the distortion correction model.

Abstract: A magnetic tracking device includes a sensor configured to generate a sensor electromotive force (EMF). The device includes a mechanism configured to select between a first operating mode in which the sensor generates the sensor EMF when receiving the magnetic field and a second operating mode in which the sensor generates a reduced amount of the sensor EMF when receiving the magnetic field. An interconnecting circuit generates a parasitic EMF in each of the first operating mode and the second operating mode. The interconnecting circuit connects to a processing device which receives a first measurement for the first operating mode, the first measurement representing the sensor EMF and the parasitic EMF, receives a second measurement for the second operating mode, the second measurement representing the parasitic EMF, compares the first measurement and the second measurement, and determines an approximate value of the sensor EMF.

Abstract: A method performed by a computing system comprises receiving a collected set of spatial information for a distal portion of an instrument at a plurality of locations within a set of anatomic passageways and receiving a set of position into for a reference portion of the instrument when the distal portion of the instrument is at each of the plurality of locations. The method also comprises determining a reference set of spatial information for the distal portion of the instrument based on the collected set of spatial information and the set of position information for the reference portion of the instrument and registering the reference set of spatial information with a set of anatomical model information.

Abstract: A system for tracking at least one bone in robotized computer-assisted surgery, comprises a processing unit and a non-transitory computer-readable memory communicatively coupled to the processing unit and comprising computer-readable program instructions executable by the processing unit for: obtaining backscatter images of the at least one bone from a tracking device in a coordinate system; generating a three-dimensional geometry of a surface of the at least one bone from the backscatter images, the three-dimensional geometry of the surface being in the coordinate system; determining a position and orientation of the at least one bone in the coordinate system by matching the three-dimensional geometry of the surface of the at least one bone to a three-dimensional model of the bone; controlling an automated robotized variation of at least one of a position and orientation of the tracking device as a function of a processing of the backscatter images; and continuously outputting the position and orientation of

Abstract: A surgical support system including: a surgical data generating apparatus operable to generate surgical data associated with a surgical procedure; and a data processing apparatus operable to: determine artificial intelligence (AI) assistance information using the generated surgical data; and provide the determined AI assistance information to a user.

Abstract: A surgical robotic system includes a ceiling mount assembly and a plurality of robotic arms coupled to a ceiling of an operating room via the ceiling mount assembly.

Abstract: A system for endoscopic surgery, comprising a first robotic arm defining the pose of an endoscopic camera, a second robotic arm defining the pose of a surgical end effector, and an irrigation nozzle configured to inject fluid under a predetermined pressure into a preselected tissue region, to generate a cavity at a surgical site. The cavity enables the camera to take images of the features of the surgical site. A controller is used to control both robotic arms, such that the pose of the endoscopic camera and the pose of the surgical end effector are known to the controller. The camera can then acquire intraoperative images of the cavity, such that an endoscopic operation can be performed in the cavity with the surgical end effector guided using the intraoperative images. Anatomic features imaged intraoperatively by the camera can be identified from preoperative images, using image registration.

Abstract: Medical robot systems, surgical tool assemblies, devices, and methods regarding the same. The medical robot system may include a robot coupled to an end-effector having a guide tube. The robot may be configured for controlled movement and positioning of the end-effector. The system further includes a motor assembly coupled to the robot. The motor assembly may be configured to move the end-effector along one or more of an x-axis, a y-axis, and a z-axis. The surgical instrument is positionable and/or slidable within the guide tube. The surgical instrument includes at least one detectable feature, such as a reflective lens or stripe. A detection device is configured and arranged to detect the at least one detectable feature. The system enables a depth of the surgical instrument in the guide tube to be determined by the at least one detectable feature on the instrument.

Abstract: A system is provided including a reclosable storage container comprising an interior sterile environment. The system also includes a sterile teleoperated component of a teleoperated surgical manipulator assembly in the interior sterile environment. A communications interface enables communication between a device outside the storage container and the component inside the storage container. A viewing window allows the stored component to be seen through the storage container. Multiple storage containers can be moved and stored. In an operating room, the storage container is opened, and the component is removed and assembled into the teleoperated surgical assembly.

Abstract: A teleoperational system receives a movement command in response to movement of an input device, in response to determining an instrument is being controlled based on the movement of the input device, maps the movement command to a first movement of the instrument in an instrument frame using a first mapping, and in response to determining a tissue probe is being controlled based on the movement of the input device, maps the movement command to a second movement of the tissue probe in a tissue probe frame using a second mapping. The first mapping maps motion in an input direction in the input frame to an instrument direction in the instrument frame. The second mapping maps motion in the input direction to a tissue probe direction in the tissue probe frame. The instrument direction corresponding with the input direction. The tissue probe direction not corresponding with the input direction.

Abstract: A medical instrument for surgery includes at least one frame and at least one jointed device. The jointed device includes at least one first joint member, or first link, adapted to connect to at least one portion of the frame and at least one second joint member, or second link. The first joint member is connected by a rotational joint to the second joint member. The medical instrument includes at least a pair of tendons, adapted to move the second joint member with respect to the first joint member. Each of the first joint member and the second joint member includes a main structural body made in a single piece with one or more convex contact surfaces. Each of the convex contact surfaces is a ruled surface formed by straight line portions all parallel to each other and substantially parallel to a joint movement axis.

Abstract: A medical instrument for surgery includes at least one frame and at least one jointed device. The jointed device includes at least one first joint member, or first link, adapted to connect to at least one portion of the frame and at least one second joint member, or second link. The first joint member is connected by a rotational joint to the second joint member. The medical instrument includes at least a pair of tendons, adapted to move the second joint member with respect to the first joint member. Each of the first joint member and the second joint member includes a main structural body made in a single piece with one or more convex contact surfaces. Each of the convex contact surfaces is a ruled surface formed by straight line portions all parallel to each other and substantially parallel to a joint movement axis.

Abstract: Robotic devices and methods for performing minimally invasive procedures on the vascular system, particularly cerebrovascular and endovascular neurosurgical procedures, where a submillimeter-scale continuum robotic device is configured and adapted for active steering and navigation based on external magnetic actuation. The submillimeter-scale continuum robotic device includes an elongate body having an inner core and an outer shell, where the outer shell is fabricated of an elastomeric material having a plurality of ferromagnetic particles dispersed therein.

Abstract: A packaging assembly may retain a sterile medical device for use in a surgical setting, such as an orthopedic implant or instrument. The packaging assembly may have a first packaging component and a second packaging component. The first packaging component and the second packaging component may be attachable to each other to define a first interior space containing the medical device. The first packaging component may have a first retention feature that defines a first interior receptacle shaped to receive at least part of the medical device such that a user can manually grip the medical device through the first retention feature. The first first interior space may be manually opened by a user grasping the medical device through the first retention feature.

Abstract: Surgical instrument trays and related methods are described. The surgical instrument tray includes a tray having a plurality of side walls and a base which define an interior space. An insert is located within the interior space of the tray and is removable from the interior space. A lid is provided for closing the interior space and which is removable from the tray. The insert has an upper surface including a plurality of outlines, each outline having the shape of the outline of a corresponding surgical instrument or part of a surgical instrument, each outline being in the form of a continuous strip, and wherein each outline has at least one support arranged to receive and releasably hold the corresponding surgical instrument or part of the surgical instrument above and in registration with the outline.

Abstract: The limiting device includes a clamping portion and a movable portion; the clamping portion and the movable portion are both annular structures, two ends of the clamping portion and the movable portion are respectively connected to form a connected double-ring structure, and the ring diameter of the movable portion is larger than that of the clamping portion. The limiting device is disposed on a core rod, the clamping portion and the core rod are in interference fit, and the movable portion and the core rod are in clearance fit. When the movable portion cooperates with the core rod, the limiting device may slide relative to the core rod; when the clamping portion cooperates with the core rod, the limiting device and the core rod are in a fixed state, and the limiting device cannot slide relative to the core rod, thus achieving the purpose of limiting.

Abstract: A system and/or method for isolating respiratory excretions from a patient during a medical procedure performed on the airways of a patient. A shield device includes a barrier, one or more support arms, and an access port. The barrier can be a flexible material, and is impervious to air. The support arm(s) maintain the barrier in a deployed state for placement over a patient's head, including the patient's mouth and nose being located within an isolation region established by the barrier. The access port is carried by the barrier and is configured to permit sealed passage of a medical device (e.g., an endoscope) into the isolation region for interfacing with the patient's airway.

Abstract: The present invention is a group of surgical instruments with improved function and design for dental and craniofacial surgery, especially subperiosteal tunneling and related procedures. The instruments include surgical elevators for vestibular incision or incisions in the gingival sulcus. The instruments have varying angles and shapes to create a mucosal tunnel in any oral or maxillofacial region. The instrument suite also optionally includes specially designed forceps for introduction of graft material inside the subperiosteal tunnel and to assist with suturing of the graft to surrounding tissue.

Abstract: A camera tracking system for computer assisted navigation during surgery operatively determines a first pose of a second extended-reality (XR) headset relative to stereo tracking cameras located on a first XR headset based on first tracking information from the stereo tracking cameras. The camera tracking system determines a second pose of eyes of a user wearing the second XR headset relative to the stereo tracking cameras located on the first XR headset based on second tracking information from the stereo tracking cameras. The camera tracking system also calibrates an eye-to-display relationship defining pose of the eyes of the user wearing the second XR headset to a display device of the second XR headset based on the determined first and second poses. The camera tracking system also controls where symbols are displayed on the display device of the second XR headset based on the eye-to-display relationship.

Abstract: Medical imaging equipment and a medical imaging method are provided. The medical imaging equipment includes medical equipment, a controller, and a head-mounted display. The medical equipment is configured to investigate a body portion and output a first image signal corresponding to the body portion. The first image signal has a first resolution. The controller is coupled to the medical equipment to receive the first image signal and convert the first resolution of the first image signal to a second image signal having a second resolution. The head-mounted display is coupled to the controller to display a display image of the second image signal. The head-mounted display has a direction line. When the head-mounted display faces the body portion, the display image and the body portion are located along to the direction line.

Abstract: Methods and devices for removing non-viable tissue at a treatment situs are described. The method can include administering a selective biofilm stain dye to the treatment situs at a dilution that selectively stains non-viable tissue compared to viable tissue at a selectivity ratio that provides a visually identifiable separation between the non-viable tissue and the viable tissue. The selective biofilm stain dye is diluted in water to a concentration of from about 0.001 mg/mL to about 0.5 mg/mL. The method can also include visually identifying the non-viable tissue, and removing the non-viable tissue based on the visual identification. A biofilm staining device can include an applicator having a dispense tip, a rupture lever adapted to rupture a rupturable capsule and release a selective biofilm stain dye, and a housing sized to retain the rupturable capsule and adapted to allow released selective biofilm stain dye to flow to the dispense tip.

Abstract: A medical chair protective barrier and gas distribution system provides a frame that forms a sealed environment for a medical gas delivered to head of a dental chair. The frame fastens to the medical chair, or rolls to head of medical chair. A laminar flow subassembly secures to frame. The laminar flow subassembly includes a vacuum pump, tubing, positive and negative pressure ports, and a vent for delivering medical gas to the head of medical chair. The frame carries a hood that covers the head of medical chair. The hood retains medical gases in a sealed environment, while protecting dentist from contact with medical gases. The hood includes a window and a pair of arm passages that regulates access to inside of hood. Medical armamentarium hangs on frame for access. System has inlet and outlet vacuum ports that utilize HEPA filters and hidden UV lights for disinfecting under the hood.