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.
Medical Device Manufacturer
Norwood Medical focuses exclusively on medical device manufacturing. We have over 40 years experience helping customers deliver innovative products to market with speed and lean manufacturing practices.
- Vertically integrated to solve problems quickly
- Focused quality processes assure excellence
In an industry that demands the highest precision to ensure the safety and wellness of medical patients, Norwood Medical understands and accepts its critical role in this supply chain.
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 13485:2003 certified
- Deploying ASQ Certified Six Sigma Black Belt Staff
- Utilizing ISO 14971:2007 risk management system for medical devices