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Nidek Co. Ltd.

Latest From Nidek Co. Ltd.

FDA 2013 Medical Device Quality-Related Warning Letters

Complete list of 76 foreign and 74 domestic device quality-related warning letters released by the agency last year.

Medical Device Compliance

FDA Warning Letters

Maker of Microfuse Putty cited for QS and MDR reg violations; Northern Digital failed to conduct process validation activities after relocating manufacturing to Mexico. Eleven warning letters listed by FDA from Oct. 8 through Nov. 11.

Medical Device Compliance

ESCRS 2009: The Next Wave in Cataract and Presbyopia Devices

The 2009 Congress of the European Society of Cataract and Refractive Surgeons and Presbyopia International 2009 Symposium took place against a backdrop of relative optimism within the refractive surgery industry. There are signs that the laser vision correction market may have hit bottom during the middle of 2009.
Medical Device

Refractive Surgery

For the ultimate in convenience, hundreds of thousands of nearsighted and farsighted patients are turning to refractive surgery, or surgical vision correction procedures that promise a permanent alternative to glasses. New companies that wish to grab a portion of the $12 billion US market for vision correction are avoiding the crowded and competitive excimer laser business, with technologies that treat patients that LASIK (laser in-situ keratomileusis) doesn't serve well.
Medical Device
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Company Information

  • Industry
  • Medical Devices
  • Pharmaceuticals
  • Therapeutic Areas
  • Ophthalmic
  • Alias(es)
  • Ownership
  • Private
  • Headquarters
  • Worldwide
    • Asia
      • Pacific Rim
        • Japan
  • Parent & Subsidiaries
  • Nidek Co. Ltd.
  • Senior Management
  • Contact Info
  • Nidek Co. Ltd.
    Phone: (81) 533 67 6611
    34-14, Maehama, Hiroishi-cho