As medical devices grow more sophisticated and regulatory standards tighten, controlled manufacturing spaces have become critical. At Cadence, we’ve stepped up to this challenge by expanding our cleanroom capabilities, giving our customers exactly what they need: precision assembly, meticulous packaging, and rigorous inspection—all under carefully controlled conditions.

Expanding Cleanroom Facilities to Meet Demand

Recognizing the rising demand, we’ve expanded our ISO Class 7 and Class 8 cleanroom spaces across multiple Cadence facilities. These enhanced environments are specifically designed to meet the strict requirements of assembling sensitive medical devices, including implantable technologies and diagnostic tools.

Delivering Fully Integrated Solutions

Our cleanroom services aren’t just about assembly. We seamlessly integrate components that we manufacture in-house alongside parts supplied by our customers or third-party vendors. Our skilled teams excel in complex procedures like precision bonding, laser welding, and sterile barrier packaging, ensuring quality at every stage.

Ensuring Quality and Compliance

Cadence’s cleanroom operations are designed and maintained to ensure compliance with ISO 13485 and FDA requirements. We adhere to strict protocols to preserve product integrity, ensuring that every device we handle meets or exceeds regulatory expectations.

Helping You Deliver Life-Changing Medical Technology

Expanding our cleanroom capabilities reflects our broader commitment to operational excellence. By providing integrated, controlled-environment manufacturing solutions, Cadence empowers customers to confidently bring innovative, life-changing medical technologies to market.