ISO 13485 Certified, FDA Registered, Rose Technologies, Inc. As a Custom Medical Device Contract Manufacturer, Rose Technologies has the Engineering expertise to meet your entire medical device design, manufacturing, assembly, automation, and packaging needs. Whether you need short-term pilot runs, or long-term production in our class 10,000 clean rooms. The Rose Technologies' product/manufacturing Team of Engineers can provide prototypes, or a complete turnkey package for your new product.
We are an FDA registered contract medical device manufacturer and we are ISO 13485:2003 Certified. Our Quality system is based on the FDA's Quality System Regulation. We continue to impress new and existing customers during supplier audits. We are your Single-Source Medical Device supplier and we want to partner with you for your next new Medical Device.
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