Our Value Proposition

At Vergent Products, we are focused on predicting and preventing problems before they happen, resulting in exceptional medical device product quality. We help you reduce risk, improve patient safety, lower total cost of ownership, and shorten your product time to market.

Our Assurance of FDA Compliance

  • ISO 13485:2016 certified
  • 21 CFR Part 820 (Quality System Regulation)
  • Unique Device Identifier (UDI) capable
  • Design History File (DHF) creation
  • Device Master Record (DMR) creation & maintenance
  • Device History Record (DHR) creation & maintenance
  • Validated manufacturing processes
  • Robust employee training records & processes

Why Work With Vergent Products Team?

  • We are a 100% digital, paperless factory
  • Rapid search and retrieval for all of your serialized product data
  • Predictive and zero-defect methodologies with exceptional process control
  • Success Every Time (SET) procedures
  • Continuous improvement via sustaining engineering services
  • Product design, printed circuit board assembly (PCBA), product assembly, order fulfillment, warranty & return services under one roof
  • Responsive and flexible, yet highly disciplined process-driven team