Facilities

Having facilities in both the U.S. and Canada is advantageous for clients, allowing us to optimize material importing, component manufacturing and assembly strategies for different markets, as well as tax and tariff jurisdictions. With cross-border mirrored production, we can provide tariff-free distribution for both American and global markets. Please inquire if you’re interested in learning more.

We are ISO 13485:2016 certified and registered with the FDA & Health Canada. Our facilities have been designed exclusively for Class I, II & III Medical Device manufacturing, with over 200,000 square feet of floor space, including multiple ISO 7 (Class 10,000) Cleanrooms.