Sterling Medical Devices assisted in the development of a Class III laparoscopic imaging camera for detecting pulmonary abnormalities with major level of concern software. The software was upgraded...
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...
Preparing for GLP Guideline Regulations in Medical Device Development As you begin the process of designing, developing, and manufacturing your medical device, there are many things you must...
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.
Sterling Medical Devices performed design services for a Class III breathing pacemaker with Major Level of Concern software, intended for use by patients who have lost neurological control of respiration. This life-sustaining device is comprised of two main components: an internal passive receiver and an external controller....
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