Profile: Arthrocare Corporation designs surgical instruments that improve patient outcomes by using our internationally patented Coblation® technology. Our technology precisely dissolves target tissue and limits damage to surrounding healthy tissue. Our technology is used in surgical specialties, which include arthroscopy, spine & neurology, ear, nose & throat, cosmetic, urology, gynecology and laparoscopy/general surgery. The ArthroCare® ENT coblator II surgery system provides precise control and superior functionality during each of our ENT procedures. Using patented Coblation technology, our ENT surgery system in conjunction with our Coblator II family of plasma wands enables tissue removal through molecular disintegration. And, with its bipolar delivery of thermal energy, the Coblator II surgery system provides localized therapy quickly and effectively for tissue coagulation.

The company was founded in 1993, has revenues of < USD 1 Million, has ~20 employees and is ISO 9001, CE certified. NASDAQ:ARTC (SEC Filings)

FDA Registration Number: 3012358417
US Agent: Bob Arnott / Smith & Nephew, Inc.
Phone: +1-(901)-399-1049  E-Mail:

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• Vertebroplasty (Does Not Contain Cement) Injector (FDA Code: OAR / 888.4200) A cement dispenser is a nonpowered syringe-like device intended for use in placing bone cement (888.3027) into surgical sites.

• Vertebroplasty Bone Cement (FDA Code: NDN / 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.

• Vertebroplasty Implants