Case Study: How to Reduce Prototype Cost with 3D Printing
The challenge The medical device market is historically fueled by innovation. The robotic surgical space is an area with a lot of […]
The challenge The medical device market is historically fueled by innovation. The robotic surgical space is an area with a lot of […]
3D printing is a prototyping method that “prints” a three-dimensional physical object in layers from a digital file. Compared to traditional prototyping […]
FMEA stands for Failure Mode and Effects Analysis and is a risk management tool for identifying potential failures. FMEA assesses the severity […]
Tyler Luneski is the latest addition to Synectic’s team of talented design and development engineers. Join us, as we sit down with […]
Biocompatibility testing is the best way to evaluate medical device safety. Through biocompatibility testing, the FDA confirms that either there are none […]
Synectic is excited to announce the addition of Hope Kavulich to our growing engineering team. Hope, a recent graduate of Quinnipiac University’s […]
Listed within the FDA’s 21 CFR 820 are detailed regulations governing medical device records and quality systems. These regulations identify five record […]
Faced with overwhelming company growth, Synectic’s parent company, Mack Molding, recently expanded its northern division by leasing 25,000 square feet in Shaftsbury, […]
21 CFR Part 820 is a set of FDA regulations that govern medical device quality systems. Detailed within are current good manufacturing practice […]
Part of the Medical Device Regulation Act involved establishing specific regulatory controls for each of the three classes of medical devices. The […]
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