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
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