Gcmedica Enterprise Ltd.
Gcmedica Enterprise Ltd.
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About GCMEDICA

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Company Profile

GCMEDICA was established in 1998 and specializes in making molds for various medical components. They supply these components to factories that specialize in manufacturing medical devices since the beginning of their foundation.


In 2002, GCMEDICA registered with the Chinese FDA and obtained permission and certification to produce disposable medical devices. Located in the New Industrial Zone of Wuxi, GCMEDICA purchased a manufacturing base covering an area of 10,000 m2, which includes a 4,500 m2 clean room with a class rating of 100,000 and well-equipped laboratories. GCMEDICA mainly produces Class II and Class I disposable medical devices, with anesthesia and respiratory products being their main focus.


GCMEDICA is equipped with a professional team that has rich experience in developing disposable medical devices and advanced molds. GCMEDICA owns various products with CE certificates and is registered with the US FDA. Through persistent and diligent exploration, GCMEDICA has expanded its product range to include urology, surgery, and gynecology products.


At GCMEDICA, we strictly adhere to a human-oriented philosophy and continuously strive to offer high-quality products and first-rate services. With our customer-first management concept, our goal is to provide extensive service and strong support to our customers at all times.

  • OUR VISION
    OUR VISION

    Concentrate carefully on medical device development, refine production and quality management for decades. Strive to shape GCMEDICA into a conscientious enterprise offering secure apparatus for the century.

  • OUR MISSION
    OUR MISSION

    Offering high-quality, secure and professional medical products and services.


  • OUR SPIRIT
    OUR SPIRIT

    GCMEDICA upholds "Integrity, Quality and Scientific Innovation" as its spirit of enterprise.


Our History

  • 2018

    Build up a new facility in Wuxi.


  • 2016

    Passed second on-site FDA audit


  • 2013

    Passed on-site strict audit by US FDA


  • 2012

    Started Japanese/Australia Marketing, Won Japan FMA certificate


  • 2010

    Expanded workshop


  • 2007

    Started American Marketing. Registered in FDA


  • 2003

    Started European marketing, Granted ISO 13485 and CE Mark


  • 2002

    Moved to Wuxi, Registered in the Chinese FDA, and got permission to produce disposable medical devices.


  • 1998

    Founded in Guandong, China