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 assisted in the development of the hardware and electronics for a strip reader that performs dry chemistry urine analysis. Sterling re-engineered the main prototype board for commercial...
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 III breathing pacemaker intended for use by patients who have lost neurological control of respiration. The pacemaker is now used...
Sterling Medical Devices participated in the development of a Class III hospital driver to support patients who’ve received an implanted heart until their condition becomes clinically stable....
Medical device manufacturers regulated by the FDA, EU, or any international regulatory agency must implement a quality management system for their medical device according to the applicable...
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.
Controller to Power Groundbreaking New Multi-Pump Mechanical Circulatory Support Device Medical Device Need A controller for an implantable heart pump that...
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