top of page
8915cf_d046f57e995d40f99e93a6d1a6799aa2~mv2.png

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 China.

​

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.

​

They are a GMP facility certified under ISO9001, ISO13485. They were the first company to be recognized by the Quality Assured Label Enterprises with the approval of China Association for Medical Devices Industry, Chinese Nursing Association, CFCP, director unit of Macromolecule Branch of China Association for Medical Devices and Vice Chairman Unit of Shenzhen Association for the Medical Devices.

​

Boon operates a state of the art facility which includes an 86,000 sq. ft. cleanroom and is located on a 12.5 acre campus.

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

Shenzhen Boon Medical Supply Factory.png

  • 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

Jiangxi.png

  • 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

trhee.png

  • 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.

Your details were sent successfully!

bottom of page