ISO 13485:2016 Certified - FDA Registered


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Medbio supports each step of the production process. We can take your medical device project from finished drawings through final assembly and packaging, meet all quality standards, provide documentation, and aid in the navigation of necessary regulatory approvals. Our flexibility allows for development and manufacturing of major projects or small, custom programs.


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Medbio Granted ISO 13485:2016 Certification

Medbio is pleased to announce they have received their certificate for the 2016 revision of the ISO 13485 standard. This... Read More →
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