Phase II Medical Manufacturing

Contract Manufacturing for Medical Devices

Founded in 1995 to serve the single-use medical product and device industry, Phase II Medical Manufacturing now provides design, development, manufacturing, packaging, shipping, and sterilization services to its customers. FDA registration, Canadian licensing, and ISO 9001:2000 and ISO 13485:2003 certification are maintained to ensure that current U.S. and international standards are satisfied.

  • Assembly Expertise
  • Manufacturing and Development
  • Complete Packaging Services
  • Offsite Warehousing and Fulfillment

FDA - ISO Certified

what people are saying...

Phase II is not just a supplier, their attention to detail coupled with their ability to respond quickly makes them an invaluable partner.

Tess Nahmiash - Senior Buyer, Medtronic Navigation