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Joint Venture Factory
DARCO-BOON GROUP

The Boon Group joined forces with DARCO International Corporation through a Joint Venture agreement utilizing DARCO’s global sales and marketing relationships to promote Boon’s manufacturing services. DARCO is a US based global sales and marketing company providing quality products to the healthcare industry with over 30 years of manufacturing experience in APAC.

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Boon was founded in 1990 and is a comprehensive manufacturing enterprise integrating product development, production, sales and service of disposable sterile medical consumables. Boon is fully licensed to manufacture under FDA, CE, CFDA and Canada MDL. The company manufactures disposable sterilized angiographic syringes, high pressure radiography injectors and accessories, infusion pump apparatus, automatic exhaust infusion sets, sterile injection needles, intravenous infusion needles, vacuum blood tubes (vein blood specimen collection devices), vein blood taking needles, vaginal dilators and specimen bags.

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The facilities are GMP certified and operate under ISO9001 and ISO13485 quality management systems. They were the first company in the APAC region to be recognized as a Quality Assured Label Enterprise with approvals from the Association for Medical Devices Industry, the Nursing Association, CFCP, the director unit of the Macromolecule Branch of the Association for Medical Devices, and the Vice Chairman Unit of the Shenzhen Association for Medical Devices.

Inside the Factory

This provides an inside look into the DARCO–Boon Group joint venture, highlighting manufacturing capabilities, quality systems, and the infrastructure supporting regulated medical device production for global markets.

1

Shenzhen Boon Medical Supply Factory

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  • 86,000‑square‑foot manufacturing facility. 
     

  • Class 8 cleanrooms with validated packaging integrity and EO sterilization.
     

  • U.S. FDA registered importer operating under ISO 13485 and FDA 21 CFR Part 820 quality systems.

2

Jiangxi Fuzhou
Factory

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  • 86,000‑square‑foot manufacturing facility. 
     

  • Class 8 cleanrooms with validated packaging integrity and EO sterilization.
     

  • U.S. FDA registered importer operating under ISO 13485 and FDA 21 CFR Part 820 quality systems.

3

Coming Soon:
Thailand Factory

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  • 90,000‑square‑foot manufacturing facility. 
     

  • Class 8 cleanrooms with validated packaging integrity and EO sterilization.
     

  • U.S. FDA registered importer operating under ISO 13485 and FDA 21 CFR Part 820 quality systems.

​Start a Manufacturing Discussion

Share your project details and our team will evaluate how the DARCO–Boon Group manufacturing services can support your requirements.

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