Product Overview
Engineering Services-Regulatory/Safety
Medical Device
Our engineers have many years of experience developing successful medical devices in conformance with the evolving worldwide medical device regulations. Pentad can help from the initial specifications through to engineering design and development, prototype verification, validation, and support of your submittal process. We work with accredited test labs to obtain the necessary regulatory, Safety, EMC, and environmental test reports. We can work with large or small clients including start-ups. Class I, II, or III; 510(k) or PMA; FDA, Canada, Europe, or worldwide; Pentad can help you develop it, make it work, obtain regulatory and marketing clearance, and support your production handoff.
Commercial Aerospace
Pentad Design has significant experience in commercial aircraft passenger cabin systems. We can help with the initial specifications, through engineering design and development, test planning, prototype verification, and final validation. We can also work within your test facilities or with accredited test labs to obtain the additional Safety, EMC, and environmental test reports.
Expertise also includes:
Commercial Products
Hazardous / Classified Locations
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