Abstract: A safety pen needle assembly (12) is disclosed which comprises a hub (30), a needle cannula (20) engaged to the hub (30), the needle cannula (20) having a distal end for insertion into a patient, and a proximal end extending into the hub (30), a sleeve (14) surrounding the hub (30) and needle cannula (20), a shield (16) including a window (18), the shield (16) surrounding the sleeve (14) and movable relative to the sleeve (14) from a first position, to a second position and to a third position to expose and cover the distal end of the needle cannula (20), and a spring (144) urging the shield (16) to move relative to the sleeve (14) from the second position to the third position, wherein the window (18) indicates when the needle cannula (20) is extended in the second position.

Abstract: A safety pen needle assembly (12) is disclosed which comprises a hub (30), a needle cannula (20) engaged to the hub (30), the needle cannula (20) having a distal end for insertion into a patient, and a proximal end extending into the hub (30), a sleeve (14) surrounding the hub (30) and needle cannula (20), a shield (16) including a window (18), the shield (16) surrounding the sleeve (14) and movable relative to the sleeve (14) from a first position, to a second position and to a third position to expose and cover the distal end of the needle cannula (20), and a spring (144) urging the shield (16) to move relative to the sleeve (14) from the second position to the third position, wherein the window (18) indicates when the needle cannula (20) is extended in the second position.

Abstract: A drug vial safety device, including a cover that is securable to a drug vial is disclosed. The cover at least partially encloses at least a neck and a lid of the drug vial. The cover includes a port having a shape that restricts syringe access to the vial through the port to a syringe shaped to be compatible with the port shape.

Abstract: A drug vial safety device, including a cover that is securable to a drug vial is disclosed. The cover at least partially encloses at least a neck and a lid of the drug vial. The cover includes a port having a shape that restricts syringe access to the vial through the port to a syringe shaped to be compatible with the port shape.

Abstract: Formed compositions for application to a bone surface of a human or animal subject, comprising: a bone material; and a carrier comprising denatured demineralized bone, where the composition is formed into a shape suitable for administration to the bone. Methods are provided for making formed compositions for application to a bone surface of a human or animal subject comprise mixing a demineralized bone and water; heating the mixture to form a carrier; mixing the carrier with bone to form a moldable composition; and molding the moldable composition to produce a formed composition. Several apparatuses are provided in which to hydrate the formed bone composition. Methods of hydrating a formed bone composition are also provided.

Abstract: A bone aspiration needle is provided. The cannulated body can define at least a first aperture for aspirating bone marrow from a first region of an anatomy. The bone aspiration needle can also include a second aperture for aspirating bone marrow from a second region of the anatomy and a third aperture for aspirating bone marrow from a third region of the anatomy. The first aperture can be a distal most aperture and the third aperture can be a proximal most aperture. The first aperture can have a first area, the second aperture can have a second area, and the third aperture can have a third area. The second area can be greater than the first area and less than the third area so as to enable the aspiration of substantially equal amounts of bone marrow substantially simultaneously from each of the first aperture, second aperture and third aperture.

Abstract: Formed compositions for application to a bone surface of a human or animal subject, comprising: a bone material; and a carrier comprising denatured demineralized bone, where the composition is formed into a shape suitable for administration to the bone. Methods are provided for making formed compositions for application to a bone surface of a human or animal subject comprise mixing a demineralized bone and water; heating the mixture to form a carrier; mixing the carrier with bone to form a moldable composition; and molding the moldable composition to produce a formed composition. Several apparatuses are provided in which to hydrate the formed bone composition. Methods of hydrating a formed bone composition are also provided.