Profile: Hologic Inc develops, manufactures and supplies premium diagnostic & medical imaging systems dedicated to serve the healthcare needs of women. We produce digital imaging technology for general radiography and mammography applications. Our Selenia uses selenium based direct capture technology that eliminates light diffusion completely for perfect clarity and exquisite image quality. We offer products such as digital mammography, analog mammography, breast biopsy, CAD and film digitizers, bone densitometry, fluoroscan mini C-arm, surgical products, diagnostic cytology, extremity MRI, general radiography, biomed training & hologic iStore. We offer customers an opportunity to enroll their bio-medical engineers into one or more of our world-class service training programs. Our training programs provide bio-medical engineers with the knowledge and confidence to be successful when servicing our products. Our training programs optimize a students learning experience by providing a quality balance of lecture, lab and hands-on experience with the product.

The company was founded in 1985. NASDAQ:HOLX (SEC Filings)

FDA Registration Number: 1220984

51 to 100 of 100 Products/Services (Click for related suppliers)  Page: 1 [2]

• Mammographic X-Ray System (FDA Code: IZH / 892.1710) A mammographic x-ray system is a device intended to be used to produce radiographs of the breast. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

• Mammographic X-Ray System Full Field Digital (FDA Code: MUE / 892.1715) A full-field digital mammography system is a device intended to produce planar digital x-ray images of the entire breast. This generic type of device may include digital mammography acquisition software, full-field digital image receptor, acquisition workstation, automatic exposure control, image processing and reconstruction programs, patient and equipment supports, component parts, and accessories.

• Mammography Devices

• Manual Radionuclide Applicator (FDA Code: IWJ / 892.5650) A manual radionuclide applicator system is a manually operated device intended to apply a radionuclide source into the body or to the surface of the body for radiation therapy. This generic type of device may include patient and equipment supports, component parts, treatment planning computer programs, and accessories.

• Medical Image Analyzer (FDA Code: MYN)

• Medical Imaging

• Medical Imaging Kits

• Medical Imaging Systems

• Microscope Slides (FDA Code: KEW / 864.3010) Tissue processing equipment consists of devices used to prepare human tissue specimens for diagnostic histological examination by processing specimens through the various stages of decalcifying, infiltrating, sectioning, and mounting on microscope slides.

• Microscope Slides (FDA Code: KEW / 864.3010)

• Mobile C-arm Fluoroscopy Systems

• Mobile Fluoroscopic X-Ray System (FDA Code: IZL / 892.1720) A mobile x-ray system is a transportable device system intended to be used to generate and control x-ray for diagnostic procedures. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

• Mobile X-Ray System (FDA Code: IZL / 892.1720)

• Motorized Mobile X-Ray System

• Needles

• Needles & Needle Guidance Systems

• Osteoporosis Care

• Papanicolau Stain (FDA Code: HZJ / 864.1850) Dye and chemical solution stains for medical purposes are mixtures of synthetic or natural dyes or nondye chemicals in solutions used in staining cells and tissues for diagnostic histopathology, cytopathology, or hematology.

• Paraffin Melting Point Apparatus (FDA Code: IDT / 864.3010)

• Pipetting and Diluting Station (FDA Code: JQW / 862.2750) A pipetting and diluting system for clinical use is a device intended to provide an accurately measured volume of liquid at a specified temperature for use in certain test procedures. This generic type of device system includes serial, manual, automated, and semi-automated dilutors, pipettors, dispensers, and pipetting stations.

• Portable Fluoroscopes

• Portable Fluoroscopes, DICOM

• Portable Fluoroscopes, Digital

• Pulsed Fluoroscopy Systems

• Radiation Therapy System

• Radiographic Anthropomorphic Phantom (FDA Code: IXG / 892.1950) A radiographic anthropomorphic phantom is a device intended for medical purposes to simulate a human body for positioning radiographic equipment.

• Radiographic Film Marking X-Ray System (FDA Code: JAC / 892.1640) A radiographic film marking system is a device intended for medical purposes to add identification and other information onto radiographic film by means of exposure to visible light.

• Radiologic Table (FDA Code: KXJ / 892.1980) A radiologic table is a device intended for medical purposes to support a patient during radiologic procedures. The table may be fixed or tilting and may be electrically powered.

• Radiological Digital Image Communication System (FDA Code: LMD / 892.2020) A medical image communications device provides electronic transfer of medical image data between medical devices. It may include a physical communications medium, modems, interfaces, and a communications protocol.

• Radiological Image Processing System (FDA Code: LLZ / 892.2050) A picture archiving and communications system is a device that provides one or more capabilities relating to the acceptance, transfer, display, storage, and digital processing of medical images. Its hardware components may include workstations, digitizers, communications devices, computers, video monitors, magnetic, optical disk, or other digital data storage devices, and hardcopy devices. The software components may provide functions for performing operations related to image manipulation, enhancement, compression or quantification.

• Radiology Workstations

• Radionuclide Brachytherapy Source (FDA Code: KXK / 892.5730) A radionuclide brachytherapy source is a device that consists of a radionuclide which may be enclosed in a sealed container made of gold, titanium, stainless steel, or platinum and intended for medical purposes to be placed onto a body surface or into a body cavity or tissue as a source of nuclear radiation for therapy.

• Remote-Controlled Radionuclide Applicator System (FDA Code: JAQ / 892.5700) A remote controlled radionuclide applicator system is an electromechanical or pneumatic device intended to enable an operator to apply, by remote control, a radionuclide source into the body or to the surface of the body for radiation therapy. This generic type of device may include patient and equipment supports, component parts, treatment planning computer programs, and accessories.

• Screen Film Mammography

• Single Lumen Hypodermic Needle (FDA Code: FMI / 880.5570) A hypodermic single lumen needle is a device intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. The device consists of a metal tube that is sharpened at one end and at the other end joined to a female connector (hub) designed to mate with a male connector (nozzle) of a piston syringe or an intravascular administration set.

• Solid State X-Ray Imager (FDA Code: MQB / 892.1680) An image-intensified fluoroscopic x-ray system is a device intended to visualize anatomical structures by converting a pattern of x-radiation into a visible image through electronic amplification. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

• Specimen Collection Device (FDA Code: LIO / 866.2900) A microbiological specimen collection and transport device is a specimen collecting chamber intended for medical purposes to preserve the viability or integrity of microorganisms in specimens during storage of specimens after their collection and during their transport from the collecting area to the laboratory. The device may be labeled or otherwise represented as sterile. The device aids in the diagnosis of disease caused by pathogenic microorganisms.

• Stationary X-Ray System (FDA Code: KPR / 892.1680)

• Surgical Needle Guide (FDA Code: GDF / 878.4800) A manual surgical instrument for general use is a nonpowered, hand-held, or hand-manipulated device, either reusable or disposable, intended to be used in various general surgical procedures. The device includes the applicator, clip applier, biopsy brush, manual dermabrasion brush, scrub brush, cannula, ligature carrier, chisel, clamp, contractor, curette, cutter, dissector, elevator, skin graft expander, file, forceps, gouge, instrument guide, needle guide, hammer, hemostat, amputation hook, ligature passing and knot-tying instrument, knife, blood lancet, mallet, disposable or reusable aspiration and injection needle, disposable or reusable suturing needle, osteotome, pliers, rasp, retainer, retractor, saw, scalpel blade, scalpel handle, one-piece scalpel, snare, spatula, stapler, disposable or reusable stripper, stylet, suturing apparatus for the stomach and intestine, measuring tape, and calipers. A surgical instrument that has specialized uses in a specific medical specialty is classified in separate regulations in parts 868 through 892.

• Surgical Trays (FDA Code: LRP / 878.4800)

• Surgical Trays (FDA Code: LRP / 878.4800)

• Tissue Processing Cell Collection Filter (FDA Code: KET / 864.3010)

• Transmission Gels & Liquids

• Used Fluoroscopy Systems

• Uterine Sounds (FDA Code: HHM / 884.4530) An obstetric-gynecologic specialized manual instrument is one of a group of devices used during obstetric-gynecologic procedures to perform manipulative diagnostic and surgical functions (e.g., dilating, grasping, measuring, and scraping), where structural integrity is the chief criterion of device performance. This type of device consists of the following:

• Video Based Fluoroscopy Systems

• Virtual Fluoroscopy System

• Wound Dressing Kit (FDA Code: MCY / 880.5075)

• X-Ray Equipment

• X-ray Equipment & Accessories