Sterling Medical Devices aided in the creation of an Integrated Development Environment (IDE) for the generation of defibrillator software and firmware development. First, Sterling developed a State...
Sterling Medical Devices assisted in the development of a next-generation Class III microburst stimulation system. The system includes Major level of concern software as well as a handheld device...
Sterling Medical Devices participated in the development of a Class I intraoral dental imaging system. The system uses an HD camera to provide real-time picture and video for diagnosis and patient...
Sterling Medical Devices planned and managed development of Class II preoperative planning software for orthopedic surgeons. The moderate level of concern software was developed in C, C++, and...
Understanding Form FDA 483 Observations The FDA conducts inspections on Class II and Class III medical device companies either for pre-approval before products are cleared for release, impromptu...
Startups are the lifeblood of medical device innovation. Without universities researching ways to solve pressing healthcare problems or doctors with experience in a particular field who have an idea to develop a prototype medical device that could help patients, the future technologies needed to help save lives wouldn't happen. But the long, arduous road through the FDA submission process to get market approval can take a long time and cost a lot of money without help. Sterling Medical Devices has been helping startups through the FDA approval process since 1998 without ever having a submission rejected.
Overview Paxman has been pioneering scalp cooling technology for over a quarter of a century. Paxman’s clinically proven cold cap technology has helped over 100,000 cancer patients in more than 60...
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