FDA Medical Device Establishment Registration
How is it different now?
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Did you know that recent changes to the FDA Medical Device Establishment Registration and Listing Regulations (Title 21-CFR Part 807) require that all Contract Manufactures (CM) and Contract Sterilizers register their facilities with the FDA and list all finished medical devices manufactured or sterilized at those facilities? These changes took effect October 1st 2012 and the deadline to register was January 31st, 2013.
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Swiss Machining
While some companies build their business model as a “machining house”, Cadence has installed custom machining processes to fully integrate these capabilities into a unique business process. Our swiss machining capabilities are optimized for high precision, automated manufacturing.
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