Abstract: Excess skin removal and wound closure devices, such as blepharoplasty devices and methods, are provided. An exemplary device for excising excess skin (e.g. eyelid skin) and creating wound closure includes a base, a lever mechanism coupled with the base via a lever pivot, a locking mechanism, an elongate curved first jaw member in fixed relationship with the base and having a lower serrated tissue contacting surface, an elongate curved second jaw member in movable relationship with the base and having an upper serrated tissue contacting surface. The upper serrated tissue contacting surface of the second jaw member can face toward the lower serrated tissue contacting surface of the first jaw member. The locking mechanism can be releasably engageable with the second jaw member. The pivoting actuation of the lever mechanism can cause linear movement of the second jaw member relative to the first jaw member.

Abstract: Suture systems, devices, and methods to enhance the precision and efficiency of surgical procedures are disclosed herein. Exemplary sutures are integrated with length indicators along their length, providing surgeons with an immediate visual reference for measuring anatomical distances intra-operatively in open and key hole (e.g. arthroscopic and endoscopic) procedures, tissue dimensions, gauging suture tension, and determining the optimal or desired suture length required for closure. The length indicators, marked at predetermined intervals, allow for accurate measurement without the need for additional tools, thereby streamlining the surgical process and reducing operation time. This suture material is particularly beneficial in complex surgeries where precision is paramount, and can improve patient outcomes by enabling more accurate tissue approximation and wound closure.

Abstract: An air-guiding device for a motor vehicle has a wheel spoiler which is arrangeable in front of a wheel of the motor vehicle in the vehicle longitudinal direction and, when in the installed position, protrudes downwards in the vehicle vertical direction relative to an adjacent underfloor region of the motor vehicle and has, on its downwardly facing side, an air-guiding edge which has a straight, first length region and a non-straight, second length region. The straight, first length region directly adjoins the non-straight, second length region inwardly in the vehicle transverse direction in the installed position, the second length region at least partially covered to the rear in the vehicle longitudinal direction by the wheel in its straight-ahead position when the wheel spoiler is in the installed position. The non-straight, second length region has multiple elevations and depressions following one another alternatingly in the vehicle transverse direction.

Abstract: An orthopedic system for delivery of a therapeutic agent to a bone includes an elongate stem adapted to be inserted into an intramedullary canal, an inlet configured to receive the therapeutic agent, and one or more outlets configured to deliver the therapeutic agent to the bone. The elongate stem may comprise one or more protrusions to engage the bone, and one or more channels extending longitudinally therein, fluidly coupled to the inlet. The therapeutic agent flows from the inlet through the one or more channels and exits into the intramedullary canal through the one or more outlets. The system may be configured to allow one or more dimensions of the system to be adjusted to accommodate the anatomy of a patient.

Abstract: Excess skin removal and wound closure devices, such as blepharoplasty devices and methods, are provided. An exemplary device for excising excess skin (e.g. eyelid skin) and creating wound closure includes a base, a lever mechanism coupled with the base via a lever pivot, a locking mechanism, an elongate curved first jaw member in fixed relationship with the base and having a lower serrated tissue contacting surface, an elongate curved second jaw member in movable relationship with the base and having an upper serrated tissue contacting surface. The upper serrated tissue contacting surface of the second jaw member can face toward the lower serrated tissue contacting surface of the first jaw member. The locking mechanism can be releasably engageable with the second jaw member. The pivoting actuation of the lever mechanism can cause linear movement of the second jaw member relative to the first jaw member.

Abstract: An orthopedic system for delivery of a therapeutic agent to a bone includes an elongate stem adapted to be inserted into an intramedullary canal, an inlet configured to receive the therapeutic agent, and one or more outlets configured to deliver the therapeutic agent to the bone. The elongate stem may comprise one or more protrusions to engage the bone, and one or more channels extending longitudinally therein, fluidly coupled to the inlet. The therapeutic agent flows from the inlet through the one or more channels and exits into the intramedullary canal through the one or more outlets. The system may be configured to allow one or more dimensions of the system to be adjusted to accommodate the anatomy of a patient.

Abstract: Disclosed are speculum embodiments and related methods to comfortably dilate a woman's vaginal canal during a pelvic exam. In one aspect, a flute having retractable rods and foldable rings are provided. The flute is configured to transition between an expanded state where the proximal and distal foldable rings are in an unfolded orientation and a collapsed state where the proximal and distal foldable rings are in a folded orientation. A handle maintains the flute in the collapsed state and, in at least one embodiment, a ring collar is provided and configured to engage the flute when the flute is in the expanded state. A light source can be provided in the flute or ring collar.

Abstract: A vertebral body replacement device, dimensioned for implantation between a first and second vertebral bone is described. The vertebral body replacement device includes a superior endcap, an inferior endcap and a central core between the superior and inferior endcaps. The vertebral body replacement device further includes a fusion aperture extending through the superior and inferior endcaps and central core. The vertebral body replacement device is made of radiolucent material and can be implanted from a lateral or anterior approach to the spine.

Abstract: The present invention involves a system and methods for assembling and implanting a vertebral body implant. The vertebral body implant includes, but is not necessarily limited to, an expandable core body and endplates that can be attached at both ends. Endplates of various shapes, sizes and angles are attachable to the expandable core so that a suitable vertebral body implant can be implanted between vertebrae.

Abstract: Systems and methods for a guide assembly for introducing a bone anchor to an operative target site. The guide includes an outer sleeve and an inner sleeve. The outer sleeve has a distal anchor engaging end, a proximal end, and a central passage extending from the distal end to the proximal end. The inner sleeve may be situated in the central passage of the outer sleeve. The inner sleeve is movable being between a first position and a second position. The first position permits insertion of the bone anchor in the central passage. The second position releasably fixes the bone anchor to the guide assembly.

Abstract: Exemplary lateral suture anchor fixation systems include a lateral anchor, a lateral anchor inserter, an auxiliary or second anchor, and an auxiliary or second anchor inserter.

Abstract: An orthopedic system for delivery of a therapeutic agent to a bone includes an elongate stem adapted to be inserted into an intramedullary canal, an inlet configured to receive the therapeutic agent, and one or more outlets configured to deliver the therapeutic agent to the bone. The elongate stem may comprise one or more protrusions to engage the bone, and one or more channels extending longitudinally therein, fluidly coupled to the inlet. The therapeutic agent flows from the inlet through the one or more channels and exits into the intramedullary canal through the one or more outlets. The system may be configured to allow one or more dimensions of the system to be adjusted to accommodate the anatomy of a patient.

Abstract: The present disclosure includes examples of an implant system configured for targeted joint resurfacing in which only an area including the osteochondral defect is resected, wherein the area resected occupies an area smaller than an entire joint surface. The implant system can include a monolithic first implant with 3D printed metal and a second implant including a plastic portion overmolded onto a metal portion. The metal portion of the second implant also includes 3D printed metal. The first and/or second implants include solid metal portion(s) and porous metal portion(s). In an example, the first implant can be a femoral implant and the second implant can be a tibial implant. The first and second implants can be used on their own or in tandem.

Abstract: Systems, devices, and methods for deploying a graft to a treatment site of a patient. Exemplary systems include a device body and an insertion mechanism. The device body can have a handle and a trigger. The insertion mechanism can be in operative association with the device body, and can have an outer sheath, a support shaft disposed at least partially within the outer sheath, an expansion mechanism coupled with the support shaft, and a graft in contact with the expansion mechanism.

Abstract: Systems, devices, and methods for deploying a graft to a treatment site of a patient. Exemplary systems include a device body and an insertion mechanism. The device body can have a handle and a trigger. The insertion mechanism can be in operative association with the device body, and can have an outer sheath, a support shaft disposed at least partially within the outer sheath, an expansion mechanism coupled with the support shaft, and a graft in contact with the expansion mechanism.

Abstract: Systems, devices, and methods for deploying a graft to a treatment site of a patient. Exemplary systems include a device body and an insertion mechanism. The device body can have a handle and a trigger. The insertion mechanism can be in operative association with the device body, and can have an outer sheath, a support shaft disposed at least partially within the outer sheath, an expansion mechanism coupled with the support shaft, and a graft in contact with the expansion mechanism.

Abstract: A vertebral body replacement device, dimensioned for implantation between a first and second vertebral bone is described. The vertebral body replacement device includes a superior endcap, an inferior endcap and a central core between the superior and inferior endcaps. The vertebral body replacement device further includes a fusion aperture extending through the superior and inferior endcaps and central core. The vertebral body replacement device is made of radiolucent material and can be implanted from a lateral or anterior approach to the spine.

Abstract: Systems, devices, and methods for deploying a graft to a treatment site of a patient. Exemplary systems operate to fix a graft to bone or soft tissue by placing multiple anchors through the graft in different locations, with individual anchors interconnected by sutures fixing the graft to the patient tissue. Exemplary anchor assemblies include an initial anchor with a suture permanently affixed, intermediate anchors through which the running suture can pass freely after placement, and a final anchor which locks the running suture under tension once placed.

Abstract: Systems, devices, and methods for deploying a graft to a treatment site of a patient. Exemplary systems include a device body and an insertion mechanism. The device body can have a handle and a trigger, and a controller. The insertion mechanism can be in operative association with the device body, and can have an outer sheath, a central shaft disposed at least partially within the outer sheath, an expansion mechanism in operative association with the central shaft, and a graft that can be deployed by the expansion mechanism.

Abstract: An orthopedic system for delivery of a therapeutic agent to a bone includes an elongate stem adapted to be inserted into an intramedullary canal, an inlet configured to receive the therapeutic agent, and one or more outlets configured to deliver the therapeutic agent to the bone. The elongate stem may comprise one or more protrusions to engage the bone, and one or more channels extending longitudinally therein, fluidly coupled to the inlet. The therapeutic agent flows from the inlet through the one or more channels and exits into the intramedullary canal through the one or more outlets. The system may be configured to allow one or more dimensions of the system to be adjusted to accommodate the anatomy of a patient.