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If you have any questions or require additional information, please contact our Manufacturing solutions coordinator or e-mail us.
Manufacturing Solutions
Quality Assurance
ISO 13485 Certification/FDA Registration
To view a copy of our certification please click here
FDA Registration
To view our FDA Registration please visit www.fda.gov and reference our registration number: 1314417
Quality Statement
Moog Medical Devices Group designs, produces, markets, sells, and distributes medical related products, services, and technologies that improve the lives of the healthcare providers and patients who use them.
We accomplish this by expertly designing and building dependable products and services, effectively applying world-class quality standards in a compassionate, collaborative work environment, continually improving our products, services, and processes by empowering our employees.
The products we sell, the services we provide and our operations fulfill the laws and regulations that relate to our business.
Our computerized quality document systems enable our personnel to access, component specifications, Device Master Records (DMR), product drawings and specifications, and validation. Our networked multiple CAD stations employ the latest version of SolidWorks software.
Inspections
We use a broad range of equipment and SPC charting to perform inspections throughout the manufacturing process, including receiving, in-process and final stages of production.

