Abstract: An air handling and filtration/treatment system (whether portable of affixed) for the mitigation and management of airborne biological contaminants (either those pre-existing or those that may become generated) that includes a suspended air in-take assembly containing a removable filter; that includes a deflector having ducting leading to a housing assembly that includes a UV sanitizer, a fan assembly and controller; and includes an outflow assembly that includes ducting leading to a position able manifold having a plurality orifices. The manifold and deflector are laterally offset from the housing assembly and vertically aligned with each other. The manifold is positioned to encircle the bioaerosol source.

Abstract: A dental prophylactic treatment device having: a prophylactic contra-angle handpiece having a handle part extending along a longitudinal axis, a head part adjoining the handle part, a tool holder rotatably disposed in the head part and extending along an axis of rotation, wherein the longitudinal axis of the handle part and the axis of rotation of the head part are disposed at an angle to one another, and a dental tool having a tool shaft and a prophylactic treatment section, wherein the tool shaft extends from a handpiece end of the dental tool over a length up to the prophylactic treatment section, wherein at least a section of the tool shaft is detachably received in the tool holder, so that the dental tool together with the tool holder can be rotated about the axis of rotation, and wherein the length of the tool shaft is a maximum of 10.0 mm.

Abstract: A replacement head for detachable coupling to an oral care implement body. The replacement head may include a head having at least one treatment element and a tubular sleeve extending from the head and defining a cavity having an axis that receives a stem of the oral care implement body. The tubular sleeve may have a proximal edge that defines an opening into the cavity. A slot in the tubular sleeve is configured to mate with a boss of the stem of the oral care implement body. The slot may include an entry slot section extending from the proximal edge of the tubular sleeve towards the head and a locking slot section extending from the entry slot section towards the head. The locking slot section may have a first lateral wall that is oblique to the cavity axis and a second lateral wall that is parallel to the cavity axis.

Abstract: The present application discloses an oral irrigator nozzle, which comprises a nozzle, a bending part, a connector and a mixed-flow nozzle located at the lower end of the nozzle, wherein the mixed-flow nozzle is provided with a shell, and an inner cavity, wherein the inner cavity is provided with a conical through hole along the water flow direction; the conical head of the conical through hole is connected with an inverted conical through hole; the junction of the conical through hole and the inverted conical through hole forms a throat cavity; the throat cavity is provided with a through hole penetrating the throat cavity; and the end of the through hole is provided with external counterbore.

Abstract: The present invention describes a method for a U-shaped teeth brush device having a conformable shape adjusting U-shaped teethbrush module and one or more individual tooth brushes coupled to the power drive mechanism, each brush having a sensor, piezoelectric crystal and transducer and each tooth brush having a block anchor coupled to the power drive, under smart controls, an electronic control system for sensing individual tooth pressure and controlling motor transmission of vibration to prior positioned brushes, whereby a users unique mouth features can be accounted for by adjusting U-shape distal ends to fit through the users mouth and align with users teeth arch for programmatically brushing more than one tooth simultaneously.

Abstract: A perineum control device attachable to the user's undergarment, belt or similar clothing to apply pressure to the perineum to control various conditions including leakages of body fluids from the urethral, anal, and vaginal openings. The device and method comprise one or more front and rear retractors having a retractable cord supporting a bridge or band member positioned against a user's perineum. When a user puts on their undergarment, or tensioned and retractable cords exert a constant and predetermined upward compression force to an attached sanitary article (such as pads/napkins). The force pushes/pulls the article against the perineum increasing the perineum pressure above an abdominal or bladder pressure, which prevents or mitigates leakages and/or prolapses. The device keeps the article in constant close contact with the orifices of the perineum regardless of a user's vigorous movements and regardless of a user's body size, shape, and anatomical differences.

Abstract: An example embolic protection system and method of deploying an embolic protection device are provided. An example embolic protection system for deploying a device in a diseased vessel of a vasculature comprises an embolic protection device including a catheter shaft and an expandable filter provided at a distal end of the catheter shaft. The expandable filter includes a side port provided in a side wall of the expandable filter and a filter actuator located at or towards a proximal end of the embolic protection device. The filter actuator is operable to open and close a mouth of the expandable filter. A snare guide wire is also provided in some examples.

Abstract: System for gas treatment of cellular implants. The system enhances the viability and function of cellular implants, particularly those with high cellular density, for use in human or veterinary medicine. The system utilizes a miniaturized electrochemical gas generator subsystem that continuously supplies oxygen and/or hydrogen to cells within an implantable and immunoisolated cell containment subsystem to facilitate cell viability and function at high cellular density while minimizing overall implant size. The cell containment subsystem is equipped with features to allow gas delivery through porous tubing or gas-only permeable internal gas compartments within the implantable cell containment subsystem. Furthermore, the gas generator subsystem includes components that allow access to water for electrolysis while implanted, thereby promoting long-term implantability of the gas generator subsystem.

Abstract: This document describes devices for treating atherosclerosis and methods for their use. For example, this document describes stent graft devices that include a fenestration or end scallop that is advantageous for use at a bifurcation of a vessel. Specifically, a medical device with a catheter comprising an elongate shaft with a proximal balloon member at a distal end, a distal balloon at the distal end spaced apart from the proximal balloon and a lateral opening in the shaft between the proximal and distal balloon members. The device also comprises a stent graft constructed of a wire framework and cover material, and a fenestration defined through the framework. The stent graft is disposed on the proximal and distal balloon members.

Abstract: A tissue lumen stent is provided with a body having an elongated tubular configuration and a foreshortened configuration. In the foreshortened configuration, downstream and upstream ends of the body expand radially into downstream and upstream flange structures, leaving a generally cylindrical saddle region therebetween. In some embodiments, the flange structures are non-symmetrical with respect to one another. Systems and methods of using the stents are also disclosed.

Abstract: A device for manipulating an implant includes a handle coupled to a guide extending from the handle to a distal end. The device includes an engagement mechanism disposed at the distal end of the guide and configured to engage an implant. The device includes a first actuator disposed on the handle and coupled to the engagement mechanism. The first actuator causes the engagement mechanism to engage the implant. The device includes an air chamber disposed in an interior chamber of the handle and configured to hold air. The device includes a lumen coupled to the air chamber and extending along the guide to the distal end. The lumen includes an air channel extending through the lumen. The device includes a second actuator disposed on the handle. The second actuator causes the air chamber to deliver the air, via the air channel, to the distal end.

Abstract: Systems, devices, and methods are provided for the delivery of an implant into the prostatic urethra. Embodiments of delivery systems can include a delivery device for insertion into the patient and a proximal control device for use in controlling release of the implant from the delivery device.

Abstract: A method and system provide an ophthalmic device. The ophthalmic device includes an ophthalmic lens having anterior surface, a posterior surface and at least one diffractive structure including a plurality of zones. The at least one diffractive structure is for at least one of the anterior surface and the posterior surface. Each zone includes at least one echelette having a least one step height. The step height(s) are individually optimized for each zone. To compensate chromatic aberration of eye from distance to a range of vision, a greater than 2? phase step height may be employed and the step height(s) folded by a phase, which is an integer multiple of two multiplied by ?. Hence chromatic aberration of eye may be compensated to improve vision from distance to near.

Abstract: A flow diversion device for treating branch point aneurysms that includes a wire stent frame comprising a plurality of wire elements, the wire stent comprising a proximal limb and two distal limbs, wherein the proximal limb and the two distal limbs converge at a crotch of the wire stent frame. The plurality of wire elements may be braided together. The flow diversion device may have a substantially Y-shape or T-shape. The flow diversion device may be manufactured by using two tubular flow diversion devices to make a Y-shaped flow diversion device.

Abstract: A valve assembly for a medical device that includes an enclosure to store an agent, a funnel coupled to the enclosure, and configured to receive the agent via an opening of the enclosure, and a valve fluidly coupled to the enclosure and the funnel. The valve is at least partially disposed between the enclosure and the funnel, and at least a portion of the agent is received on the valve. The valve is configured to move from a first position to a second position relative to the enclosure and the funnel to selectively release the agent from the enclosure into the funnel. In the first position, the valve is configured to close the opening and inhibit the agent from exiting the enclosure and entering the funnel. In the second position, the valve is configured to open the opening and release the agent from the enclosure for delivery into the funnel.

Abstract: A transcatheter growth device for treating congenital illnesses in infantile and other pediatric heart disease patients and methods for making and using the same. The growth device includes an elongated device frame with alternating annular growth cell members and spacing members that axially span proximal and distal end regions of the device frame. The growth cell members and spacing members define a radial periphery for the growth device. Each growth cell member can comprise a scaffolded growth cell member with first and second annular strut arrangements coupled via a growth cell junction to provide device frame flexibility. A retention member for engaging a selected lumen within a patient and a covering member for sealing the growth device, when deployed, are disposed at the device periphery. The growth device advantageously can be deployed for treating heart disease alone or in combination with one or more additional growth devices.

Abstract: A prosthetic heart valve has a frame including a plurality of strut members, the frame being radially expandable and collapsible between a collapsed state and an expanded state, the frame having an inflow end and an outflow end and defining a longitudinal axis. A leaflet structure is situated at least partially within the frame. A covering is disposed around an exterior of the frame and includes a cushioning layer, a first strip of material coupled to the cushioning layer and folded to encapsulate apices of the strut members of the inflow end of the frame, and a second strip of material coupled to the cushioning layer and folded to encapsulate apices of the strut members of the outflow end of the frame. The cushioning layer includes texturized filaments that provide compressible volume and a plush surface to the cushioning layer when the frame is in the expanded state.

Abstract: Apparatuses, systems and methods for providing improved ophthalmic lenses, particularly intraocular lenses (IOLs), include features for reducing dysphotopsia effects, such as haloes and glare. Exemplary ophthalmic lenses can include an optic including a diffractive achromat configured to direct light to a common focus, with individual zones of the diffractive achromat directing light to the common focus in at least two different diffractive orders utilizing at least two different diffractive powers.

Abstract: A method can comprise deploying a prosthetic valve with a delivery apparatus, where the prosthetic valve comprises a frame and a rotatable screw connected to the frame, and where the screw comprises a screw head having an annular bore with internal threads. The delivery apparatus is releasably coupled to the screw and can comprise a first shaft and a first head disposed at an end of the first shaft, the first head comprising external threads releasably engaged with the internal threads of the screw head, and a second shaft that is coaxial with and surrounds the first shaft, the second shaft comprising a second head disposed at an end of the second shaft, the second head releasably engaged with an exterior surface of the screw head. Deploying the valve includes radially expanding the prosthetic valve by rotating the screw with the delivery apparatus.

Abstract: A transcatheter valve prosthesis and a method for implanting the prosthesis in a heart are disclosed. The prosthesis includes a tubular body a coupled to a prosthetic valve. The method includes partially deploying the tubular body from a catheter to at position distal of a junction between a leaflet part and chordae of a native valve leaflet, and moving the catheter such that the deployed outflow end portion of the tubular body engages the native valve leaflet. Then, the tubular body can be fully deployed.