Improvements for curettes currently used in debridement and removal of skin, tissue, and necrotic debris from wound beds comprising a pinchable cap and a circular metal cutting end, wherein an individual may preferably apply pressure to the cap, preferably covering the metal cutting end, in order to manipulate the cutting end into a shape to preferably debride narrow or smaller portions of a wounds such as a narrow oval. The surgical instrument also preferably includes a measurement scale, a depth probe that also acts as a packing tool, and finger grips. There can be an optional LED or LEDs included in or on the curette.

Improvements for curettes currently used in debridement and removal of skin, tissue, and necrotic debris from wound beds comprising a pinchable cap and a circular metal cutting end, wherein an individual may preferably apply pressure to the cap, preferably covering the metal cutting end, in order to manipulate the cutting end into a shape to preferably debride narrow or smaller portions of a wounds such as a narrow oval. The surgical instrument also preferably includes a measurement scale, a depth probe that also acts as a packing tool, and finger grips. There can be an optional LED or LEDs included in or on the curette.

Provided are approaches to establish a failsafe barrier to internal bleeding from percutaneous wounds to protect a patient from failed wound closure devices or related complications due to a variety of contributing factors such as state of systemic anticoagulation, errors in surgical procedure, variability in patient anatomy, and the like. Systems include a clotting agent to encase, and thus isolate, substantially the entire wound access area from the rest of the patient and an instrument, such as an intravascular introducer sheath, inserted through a wound at an access site on a vessel, for delivering the clotting agent to the entire enveloping tissue region around the accessed area as a mold cavity to be filled with the clotting agent. With benefits of patient safety, user simplicity, and low healthcare cost driving the effort, autologous whole blood is the preferred injected agent.

A bone plate has a curved elongated body including a first end portion and a second end portion. The first end portion is laterally offset relative to the second end portion, and includes a plurality of screw holes. A first screw hole is defined by the second end portion. Each of the screw holes of the first end portion are laterally offset from a straight line extending in a direction along a length dimension of the bone plate and bisecting the first screw hole of the second end portion, and each of the screw holes of the first end portion are on the same side of the straight line as one another.

The present invention provides a surgical treatment for a disordered knee in a dog, the disorder comprising a partially ruptured cranial cruciate ligament (CrCL), a fully ruptured CrCL, or a displaced patella. The methods of treatment include surgical transection of the tendon of the popliteal muscle, which reduces the in-toeing of the paw as it lands on the ground. In vitro experiments suggest that neutralization of this torque can reduce by several fold tensile forces in the CrCL or its replacement, as well as in its surrogate, a lateral suture placed extra-capsularly.

The present invention provides a surgical treatment for a disordered knee in a dog, the disorder comprising a partially ruptured cranial cruciate ligament (CrCL), a fully ruptured CrCL, or a displaced patella. The methods of treatment include surgical transection of the tendon of the popliteal muscle, which reduces the in-toeing of the paw as it lands on the ground. In vitro experiments suggest that neutralization of this torque can reduce by several fold tensile forces in the CrCL or its replacement, as well as in its surrogate, a lateral suture placed extra-capsularly.

A vascular compression apparatus and method for applying pressure onto an area of a patient generally including a blood vessel and a wound site, such as a blood vessel puncture, after a cannulated procedure for the purpose of controlling bleeding and achieving hemostasis. The vascular compression apparatus includes a handle, a shaft and a pad. The shaft extends generally downward from the center of the bottom side of the handle. The pad is connected generally off-center of its top side to the bottom end of the shaft. The bottom side of the pad is convex to allow the vascular compression device to be rocked back and forth. In use, the pad is generally placed proximal to the catheter insertion site and over the blood vessel containing the catheter. The device is rocked proximally to control blood flow while removing the catheter. After the catheter is removed from the puncture site, the device is rocked distally to the puncture site, where pressure is applied until hemostasis is achieved.

A device for treating tissue includes a capsule extending longitudinally from a proximal end to a distal end and including a lumen extending therein and a clip slidably received within the lumen of the capsule. The clip includes a middle prong, a first outer prong and a second outer prong. The first prong is coupled to the middle prong so that the first prong is movable relative to the middle prong between a first open configuration and a first closed configuration. The second outer prong coupled to the middle prong so that the second prong is movable relative to the middle prong between a second open configuration and a second closed configuration. The first and second outer prongs are independently movable relative to the middle prong to be moved between the first and second open configurations to the first and second open configurations and the first and second closed configurations.

A medical injection and suction device includes: a housing that encloses a driving motor; a syringe mount disposed on a wall of an upper side of the housing; a plurality of valves disposed on the wall of the upper side of the housing and on a side of the syringe mount; a slider that moves toward or away from the housing and is disposed on a lateral side of the housing; a driving rod connected to the slider; and at least one slide rod. The driving rod extends through a wall of the lateral side of the housing. An end of the driving rod is connected to the driving motor. The driving motor drives the driving rod to move the slider. An end of the at least one slide rod is connected to the wall of the lateral side of the housing. The slider is disposed in a slidable manner on the slide rod.

Surgical methods involving cutting and sealing tissue include affixing a first adjunct material to tissue at a treatment site, such as by stapling the adjunct to tissue. A second adjunct material is applied to at least a portion of the first adjunct material such that the second adjunct material interacts with the first adjunct material to form a seal in an area of the tissue covered by at least one of the first and the second adjunct material. The resulting tissue sealing structure, which includes a combination of the two adjuncts, is believed to be superior to the sealing properties of either adjunct alone.