Stryker Communications Corp.

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Contact: Chad Croasdale - National Director of Marketing
Web: http://www.strykercom.com
E-Mail:
Address: 1410 Lakeside Parkway, Flower Mound, Texas 75028, USA
Phone: +1-(972)-410-7100, 866-726-3705 | Fax: +1-(408)-754-2969 | Map/Directions >>

Profile: Stryker specializes in medical technology. Our expertise lies in the orthopedic market and our products help medical professionals improve the lives of their patients. We offer a variety of products and services that are designed to make things easier. We also offer many tools to help hospitals educate their communities and potential patients about surgical procedures & offer visitation programs to help hospitals advance their patient care.

The company was founded in 1999, has revenues of USD 10-25 Million, has ~150 employees. NYSE:SYK (SEC Filings)

FDA Registration Number: 2031963

37 Products/Services (Click for related suppliers)

• AC-Powered Medical Examination Device (FDA Code: KZF / 880.6320)

An AC-powered medical examination light is an AC-powered device intended for medical purposes that is used to illuminate body surfaces and cavities during a medical examination.

• AC-Powered Operating Room Table (FDA Code: FQO / 878.4960)

Operating tables and accessories and operating chairs and accessories are AC-powered or air-powered devices, usually with movable components, intended for use during diagnostic examinations or surgical procedures to support and position a patient.

• Anesthesia Table and Tray Cabinet (FDA Code: BRY / 868.6100)

An anesthetic cabinet, table, or tray is a device intended to store anesthetic equipment and drugs. The device is usually constructed to eliminate build-up of static electrical charges.

• Arthroscope Accessories

• Arthroscopes (FDA Code: HRX / 888.1100)

An arthroscope is an electrically powered endoscope intended to make visible the interior of a joint. The arthroscope and accessories also is intended to perform surgery within a joint.

• Arthroscopy Operative and Diagnostic Hardwares

• Bone Cement (FDA Code: LOD / 888.3027)

Polymethylmethacrylate (PMMA) bone cement is a device intended to be implanted that is made from methylmethacrylate, polymethylmethacrylate, esters of methacrylic acid, or copolymers containing polymethylmethacrylate and polystyrene. The device is intended for use in arthroplastic procedures of the hip, knee, and other joints for the fixation of polymer or metallic prosthetic implants to living bone.

• Ceiling Mounted Surgical Light (FDA Code: FSY / 878.4580)

A surgical lamp (including a fixture) is a device intended to be used to provide visible illumination of the surgical field or the patient.

• Endoscope Accessories (FDA Code: KOG)

• Endoscopic Light Source

• Endoscopic Video Camera

• General & Plastic Surgery Laparoscope (FDA Code: GCJ / 876.1500)

An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.

• Hip Replacement Systems

• Infrared Imaging Systems

• Injectable HA Bone Substitutes

• Integrated Arthroscopy Systems

• Knee Replacement Systems

• Laparoscopy, Laparoscopes

• Microdissection Needles

• Osteoconductive HA Bone Paste

• Partial Knee Systems

• Powered Shaver Systems

• Primary Acetabular Components

• Primary Femoral Components

• Primary Knee Systems

• 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 Digital Image Storage Device (FDA Code: LMB / 892.2010)

A medical image storage device is a device that provides electronic storage and retrieval functions for medical images. Examples include devices employing magnetic and optical discs, magnetic tape, and digital memory.

• 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.

• Revision Femoral Components

• Revision Knee Systems

• RF Ablation Systems

• Shoulder & Elbow Systems

• Soft Tissue Repair Products

• Surgical Camera and Accessories (FDA Code: KQM / 878.4160)

A surgical camera and accessories is a device intended to be used to record operative procedures.

• Trauma Navigation Systems

• Universal Wireless Footswitch Systems

• Wall Vacuum-Powered Operating Room Suction Apparatus (FDA Code: GCX / 880.6740)

A vacuum-powered body fluid suction apparatus is a device used to aspirate, remove, or sample body fluids. The device is powered by an external source of vacuum. This generic type of device includes vacuum regulators, vacuum collection bottles, suction catheters and tips, connecting flexible aspirating tubes, rigid suction tips, specimen traps, noninvasive tubing, and suction regulators (with gauge).