Medical Device Qualified Supplier Directory
Qualifications: ISO 13485, FDA Registered, CGMP Certified
Markets Supplied: North America, Europe
SanaVita Medical, LLC is a contract manufacturing partner for medical device and life science companies worldwide. Our expertise is focused on implantable biomaterials, drug-releasing implants, and combination products. Our contract manufacturing and medical device processing services include; ISO class 7 cleanroom finishing and assembly, packaging and labeling, sterilization management, and regulatory registration and compliance support. An experienced device project management team will guide your project from proof of concept through market launch including manufacturing process development and technology transfer.
At SanaVita Medical, we’re committed to working closely with you to streamline your supply chain and get your product to market smoothly and efficiently. Our unique capabilities can help bring your medical device vision to market. Technical resources available to assist customers include; equipment qualification and process validation, component coating, polymer extrusion, assistance in package design and materials sourcing, and supply chain management.
SanaVita is an FDA (21 CFR 210, 211 and 820) registered contract manufacturer with a quality management system that is compliant with ISO 13485:2016.
SanaVita Medical’s focus is solely on the healthcare industry. Therefore, we are uniquely positioned to serve both established and early-stage medical device and pharmaceutical companies. We are flexible enough to handle small volume and hand assemblies for niche markets or clinical trials. Also, larger OEM manufacturers rely on us to meet their specialized requirements.
For more information contact SanaVita Medical