Abstract: A surgical system includes an end effector assembly, a motor assembly, an energy source, and a controller. The controller activates the motor assembly, once it is determined that tissue is present between jaw members of the end effector assembly, to move the jaw members from a spaced-apart position to an approximated position to grasp tissue. The controller further activates the energy source, once tissue is grasped between the jaw members, to supply energy to the jaw members to seal tissue grasped between the jaw members. The controller further activates the motor assembly, once it is determined that tissue sealing is complete, to move the jaw members from the approximated position to the spaced-apart position to release sealed tissue. The system may further be configured to cut tissue once it is determined that tissue sealing is complete but before moving the jaw members to the spaced-apart position.

Abstract: A surgical system includes an end effector assembly, a motor assembly, an energy source, and a controller. The controller activates the motor assembly, once it is determined that tissue is present between jaw members of the end effector assembly, to move the jaw members from a spaced-apart position to an approximated position to grasp tissue. The controller further activates the energy source, once tissue is grasped between the jaw members, to supply energy to the jaw members to seal tissue grasped between the jaw members. The controller further activates the motor assembly, once it is determined that tissue sealing is complete, to move the jaw members from the approximated position to the spaced-apart position to release sealed tissue. The system may further be configured to cut tissue once it is determined that tissue sealing is complete but before moving the jaw members to the spaced-apart position.

Abstract: Medical procedure related objects (e.g., instruments, supplies) tagged with transponders (e.g., RFID transponders, dumb transponders) are accounted for in a medical or clinical environment via an accounting system using a number of antennas and interrogators/readers. A first set of antennas and RFID interrogator(s) interrogate portions of the environment for RFID tagged objects, for example proximate a start and an end of a procedure. Shielded packaging and/or shielded receptacles shield tagged objects, preventing interrogation except for those objects in unshielded portions of the environment. A shielded receptacle may include an antenna to interrogate the contents thereof in a relatively noise-free environment. A data store may maintain information including a current status or count of each instrument or supply, for instance as checked in or checked out. A handheld antenna and/or second set of antennas interrogates a body of a patient for retained instruments or supplies tagged with dumb transponders.

Abstract: Methods and systems for controlling the usage of devices with embedded RFID tags including connecting a device to an energy source and reading data from a memory device incorporated in the device. The data may include a unique identifier (UID), a usage value, an activation value, a reprocessing value, and/or a sterilization indicator. The usage value is incremented when the device is connected to the energy source and the activation value is incremented when the device is activated permitting energy to flow from the energy source to the device. Usage of the device is prevented if the UID is on a list of prohibited UIDs, the usage value is not lower than a usage limitation value, the reprocessing value equals a reprocessing limitation value, the activation value equals an activation limitation value, and/or the sterilization indicator does not indicate that the device has been sterilized since its previous usage.

Abstract: Embodiments of the present disclosure provide systems and devices for delivering gaseous Nitric Oxide (gNO) under therapeutic parameters to reduce infection in a subject. Certain embodiments include devices and systems for delivering pressurized gNO to reduce bioburden and promote healing in the wounds of subjects having various disease conditions, including skin and soft tissue infections (SSTIs) and osteomyelitis. In some embodiments, the present disclosure provides portable wound healing devices for delivering pressurized gNO to the site of a wound to treat various disease conditions in a subject. Other embodiments relate to systems and devices for delivering and for monitoring gaseous Nitric Oxide (gNO) under therapeutic parameters of use to treat a subject. In certain embodiment, the devices include a subject interface unit comprising sensors for detecting gNO pressure and/or gNO flow.

Abstract: Medical procedure related objects (e.g., instruments, supplies) tagged with transponders (e.g., RFID transponders, dumb transponders) are accounted for in a medical or clinical environment via an accounting system using a number of antennas and interrogators/readers. A first set of antennas and RFID interrogator(s) interrogate portions of the environment for RFID tagged objects, for example proximate a start and an end of a procedure. Shielded packaging and/or shielded receptacles shield tagged objects, preventing interrogation except for those objects in unshielded portions of the environment. A shielded receptacle may include an antenna to interrogate the contents thereof in a relatively noise-free environment. A data store may maintain information including a current status or count of each instrument or supply, for instance as checked in or checked out. A handheld antenna and/or second set of antennas interrogates a body of a patient for retained instruments or supplies tagged with dumb transponders.

Abstract: Headgear includes a base configured to engage the head of the wearer. A force absorbing structure is carried by the base. In some cases, the force absorbing structure includes a surface including a coarse macrostructure configured to facilitate absorbing forces applied to the headgear. The coarse macrostructure includes a plurality of protrusions, and at least one of the protrusions has a thickness of at least about 0.50 mm. In some cases, the force absorbing structure includes a porous macrostructure configured to facilitate absorbing forces applied to the headgear. The porous macrostructure includes a plurality of passageways each having a width of at least about 2.00 mm.

Abstract: Medical procedure related objects (e.g., instruments, supplies) tagged with transponders (e.g., RFID transponders, dumb transponders) are accounted for in a medical or clinical environment via an accounting system using a number of antennas and interrogators/readers. A first set of antennas and RFID interrogator(s) interrogate portions of the environment for RFID tagged objects, for example proximate a start and an end of a procedure. Shielded packaging and/or shielded receptacles shield tagged objects, preventing interrogation except for those objects in unshielded portions of the environment. A shielded receptacle may include an antenna to interrogate the contents thereof in a relatively noise-free environment. A data store may maintain information including a current status or count of each instrument or supply, for instance as checked in or checked out. A handheld antenna and/or second set of antennas interrogates a body of a patient for retained instruments or supplies tagged with dumb transponders.

Abstract: Methods and systems for controlling the usage of devices with embedded RFID tags including connecting a device to an energy source and reading data from a memory device incorporated in the device. The data may include a unique identifier (UID), a usage value, an activation value, a reprocessing value, and/or a sterilization indicator. The usage value is incremented when the device is connected to the energy source and the activation value is incremented when the device is activated permitting energy to flow from the energy source to the device. Usage of the device is prevented if the UID is on a list of prohibited UIDs, the usage value is not lower than a usage limitation value, the reprocessing value equals a reprocessing limitation value, the activation value equals an activation limitation value, and/or the sterilization indicator does not indicate that the device has been sterilized since its previous usage.

Abstract: Methods and systems for controlling the usage of devices with embedded RFID tags including connecting a device to an energy source and reading data from a memory device incorporated in the device. The data may include a unique identifier (UID), a usage value, an activation value, a reprocessing value, and/or a sterilization indicator. The usage value is incremented when the device is connected to the energy source and the activation value is incremented when the device is activated permitting energy to flow from the energy source to the device. Usage of the device is prevented if the UID is on a list of prohibited UIDs, the usage value is not lower than a usage limitation value, the reprocessing value equals a reprocessing limitation value, the activation value equals an activation limitation value, and/or the sterilization indicator does not indicate that the device has been sterilized since its previous usage.

Abstract: A microwave ablation system includes an energy source adapted to generate microwave energy and a power splitting device having an input adapted to connect to the energy source and a plurality of outputs. The plurality of outputs are configured to be coupled to a corresponding plurality of energy delivery devices. The power splitting device is configured to selectively divide energy provided from the energy source between the plurality of energy devices.

Abstract: Medical procedure related objects (e.g., instruments, supplies) tagged with transponders (e.g., RFID transponders, dumb transponders) are accounted for in a medical or clinical environment via an accounting system using a number of antennas and interrogators/readers. A first set of antennas and RFID interrogator(s) interrogate portions of the environment for RFID tagged objects, for example proximate a start and an end of a procedure. Shielded packaging and/or shielded receptacles shield tagged objects, preventing interrogation except for those objects in unshielded portions of the environment. A shielded receptacle may include an antenna to interrogate the contents thereof in a relatively noise-free environment. A data store may maintain information including a current status or count of each instrument or supply, for instance as checked in or checked out. A handheld antenna and/or second set of antennas interrogates a body of a patient for retained instruments or supplies tagged with dumb transponders.

Abstract: A microwave ablation system is disclosed. The system includes a microwave antenna assembly that includes an identification device configured to store an optimal frequency of the microwave antenna assembly. The system also includes a generator configured to couple to the microwave antenna assembly and to output microwave energy at an operational frequency. The generator is further configured to read the optimal frequency from the identification device and to configure the operational frequency to substantially match the optimal frequency.

Abstract: Embodiments of the present disclosure provide systems and devices for delivering gaseous Nitric Oxide (gNO) under therapeutic parameters to reduce infection in a subject. Certain embodiments include devices and systems for delivering pressurized gNO to reduce bioburden and promote healing in the wounds of subjects having various disease conditions, including skin and soft tissue infections (SSTIs) and osteomyelitis. In some embodiments, the present disclosure provides portable wound healing devices for delivering pressurized gNO to the site of a wound to treat various disease conditions in a subject. Other embodiments relate to systems and devices for delivering and for monitoring gaseous Nitric Oxide (gNO) under therapeutic parameters of use to treat a subject. In certain embodiment, the devices include a subject interface unit comprising sensors for detecting gNO pressure and/or gNO flow.

Abstract: A surgical system includes an end effector assembly, a motor assembly, an energy source, and a controller. The controller activates the motor assembly, once it is determined that tissue is present between jaw members of the end effector assembly, to move the jaw members from a spaced-apart position to an approximated position to grasp tissue. The controller further activates the energy source, once tissue is grasped between the jaw members, to supply energy to the jaw members to seal tissue grasped between the jaw members. The controller further activates the motor assembly, once it is determined that tissue sealing is complete, to move the jaw members from the approximated position to the spaced-apart position to release sealed tissue. The system may further be configured to cut tissue once it is determined that tissue sealing is complete but before moving the jaw members to the spaced-apart position.

Abstract: An orthotic device according to embodiments of the present invention includes a substantially rigid internal footbed with an external rocker bottom, two struts rigidly coupled to the footbed, a paddle coupled to each strut, each paddle having an inner surface configured to face a limb of a patient, and a strap system configured to interface with the paddles for tightening around the limb, the inner surfaces of the paddles including a plurality of protrusions configured to minimize sliding of the first and second paddles with respect to the limb or with respect to a cast applied to the limb. The orthotic device may include two or more support layers on the footbed, each layer having a support aperture larger than and at least partially overlapping the support aperture below.

Abstract: A surgical system includes an end effector assembly, a motor assembly, an energy source, and a controller. The controller activates the motor assembly, once it is determined that tissue is present between jaw members of the end effector assembly, to move the jaw members from a spaced-apart position to an approximated position to grasp tissue. The controller further activates the energy source, once tissue is grasped between the jaw members, to supply energy to the jaw members to seal tissue grasped between the jaw members. The controller further activates the motor assembly, once it is determined that tissue sealing is complete, to move the jaw members from the approximated position to the spaced-apart position to release sealed tissue. The system may further be configured to cut tissue once it is determined that tissue sealing is complete but before moving the jaw members to the spaced-apart position.

Abstract: Methods and systems for controlling the usage of devices with embedded RFID tags including connecting a device to an energy source and reading data from a memory device incorporated in the device. The data may include a unique identifier (UID), a usage value, an activation value, a reprocessing value, and/or a sterilization indicator. The usage value is incremented when the device is connected to the energy source and the activation value is incremented when the device is activated permitting energy to flow from the energy source to the device. Usage of the device is prevented if the UID is on a list of prohibited UlDs, the usage value is not lower than a usage limitation value, the reprocessing value equals a reprocessing limitation value, the activation value equals an activation limitation value, and/or the sterilization indicator does not indicate that the device has been sterilized since its previous usage.

Abstract: Headgear includes a base configured to engage the head of the wearer. A force absorbing structure is carried by the base. In some cases, the force absorbing structure includes a surface including a coarse macrostructure configured to facilitate absorbing forces applied to the headgear. The coarse macrostructure includes a plurality of protrusions, and at least one of the protrusions has a thickness of at least about 0.50 mm. In some cases, the force absorbing structure includes a porous macrostructure configured to facilitate absorbing forces applied to the headgear. The porous macrostructure includes a plurality of passageways each having a width of at least about 2.00 mm.

Abstract: Embodiments of the present disclosure provide systems and devices for delivering gaseous Nitrous Oxide (gNO) under therapeutic parameters to reduce infection in a subject. Certain embodiments include devices and systems for delivering pressurized gNO to reduce bioburden and promote healing in the wounds of subjects having various disease conditions, including skin and soft tissue infections (SSTIs) and osteomyelitis. In some embodiments, the present disclosure provides portable wound healing devices for delivering pressurized gNO to the site of a wound to treat various disease conditions in a subject.