Embodiments of claimed subject matter are directed to an illuminating surgical device comprising a single control element to control an array of illuminating elements and an array of louvers to direct light from the individual illuminating elements toward a surgical field.

An exemplary embodiment comprises an illuminated suction device having a distal end with a suction tip; a proximal end with a connector for a suction tube; and an illumination assembly comprising at least one light source, at least one battery and an activation device for energizing the light source, the illumination assembly being permanently attached to the suction device.

A cordless light attachment for an object includes a housing that has a proximal end and a distal end, and an interior cavity that extends from the proximal end to the distal end, forming an opening extending through the housing from the proximal end to the distal end. The device receives therein an object and removably attaches to the object. The device has at least one light source powered by a cordless power source arranged on or within the housing.

A lighting assembly includes a light transmissive substrate extending along a length and including a light emission portion including opposed first and second major surfaces spaced apart from one another in a thickness direction, an inner edge surface extending between the first and second major surfaces in the thickness direction, and an outer edge surface opposed the inner edge surface and extending in the thickness direction. An extension portion extends from the light emission portion proximate the second major surface in the thickness direction. A light source is attached to the extension portion. A light head includes a housing, a primary light source attached to the housing, and the lighting assembly as an auxiliary lighting assembly. The housing includes a channel in which the auxiliary lighting assembly is retained.

A biopsy device includes a cannula and a specimen collector. The cannula has a proximal end and a longitudinal axis. The specimen collector contains the proximal end of the cannula. The specimen collector has a removable sample receiving cartridge that is removable along the longitudinal axis of the cannula to expose the proximal end of the cannula.

A biopsy device includes a disposable elongated probe component having a coaxial arrangement of an elongated tubular section and an elongated tissue cutting member, and having a coaxial arrangement of a first driven gear, a second driven gear, and a third driven gear. The first driven gear is configured to rotate the elongated tubular section. The second driven gear is configured to rotate to longitudinally move the elongated tissue cutting member. The third driven gear is configured to rotate or oscillate the elongated tissue cutting member. A driver component has a coaxial arrangement of a first drive gear, a second drive gear, and a third drive gear. The first drive gear is drivably engaged with the first driven gear. The second drive gear is drivably engaged with the second driven gear. The third drive gear is drivably engaged with the third driven gear.

A walker caddy device for carrying items while using a walker and lighting a path in front of a user of the walker includes a caddy defining an interior space and having a support clip coupled to a back wall of the caddy. The support clip is configured to couple to an upper cross member of a walker with the caddy being supported by a lower cross member of the walker. The caddy has a light source coupled to a front wall powered by a power module for selectively lighting an area in front of the walker.

A method of inactivating one or more pathogens in an environment. The method includes providing light from at least one lighting element of a lighting device installed in the environment, the at least one lighting element configured to provide light toward a target area in the environment, the provided light having at least a pathogen-inactivating first component in a first range of wavelengths of 400 nanometers to 420 nanometers. The pathogen-inactivating first component of light produces an irradiance of at least 0.01 mW/cm.sup.2 as measured at a surface in the target area that is unshielded from the lighting device and located at a distance of 1.5 meters from an external-most luminous surface of the lighting device. Providing the light causes the one or more pathogens to be inactivated.

A method of providing doses of light sufficient to deactivate bacteria throughout a volumetric space. The method includes: (1) receiving data associated with a desired illuminance level for the space, indicative of an estimated occupancy of the volumetric space over a pre-determined period of time, and indicative of dimensions of the space; (2) determining, based on the received data, an arrangement of one or more lighting fixtures in the volumetric space, the one or more lighting fixtures configured to at least partially emit disinfecting light having a wavelength of between 400 nm and 420 nm, and a total radiometric power to be applied via the one or more lighting fixtures to produce a desired power density at any exposed surface within the volumetric space during the period of time; and (3) installing the determined arrangement of one or more lighting fixtures in the volumetric space.

Lighting devices are disclosed for use with handheld surgical instruments, along with holsters for supporting surgical instruments with lighting devices thereon and kits containing surgical instruments and lighting devices.