Assembly & Packaging
As a full-service contract manufacturer for medical device companies, Norwood Medical is equipped with the facilities and resources to provide final assembly and packaging at the industry’s highest standards. Our certifications in cleanroom operations and controlled manufacturing environments enable our customers to rely on us throughout the entire production life cycle.
Controlled manufacturing environment
Norwood Medical’s facilities are equipped with several Class 8 (100,000) controlled manufacturing environments for final assembly and packaging. Our staff is experienced in both manual and mechanical assembly processes, and our holistic approach to quality assures each component is produced at our customers’ exacting requirements.
Norwood Medical is equipped with ISO Class 7 (10,000) cleanrooms to perform assembly and packaging without exposure to environmental contaminations. Maintaining the highest medical device standards for our customers is our greatest commitment, and Norwood Medical’s cleanroom service is one of the many ways we accomplish this goal.
At Norwood Medical, all of our manufacturing, production, assembly and packaging processes are centered on the goal of delivering the highest quality medical devices for our customers. We’re motivated by the knowledge that every device we produce will ultimately contribute to the well-being of the recipient of a medical procedure.
Minimally Invasive Surgical
Norwood Medical partners with the industry’s leading medical device suppliers to aid in the progress of minimally invasive surgery. From wound closure to general surgery, we help our customers create devices that are secure and effective for a variety of procedural needs:
- Surgical Cutting and Stapling Components
- Clip Applier Components
- Harmonic Device Components
- Linear Cutter Components
- Cannula Components
Dedication to Quality
Norwood assures customer satisfaction and product safety through a robust and proven Quality System. We recognize that there is no place for implants, instruments or procedures that don’t meet the very highest quality standards
- 21 CFR 820 FDA Quality System Regulation (QSR) compliant and ISO 13485:2016 certified
- Deploying ASQ Certified Six Sigma Black Belt Staff
- Utilizing ISO 14971:2012 risk management system for medical devices