Final Inspection product inspection is a rigid requirement for regulatory compliance and market access. Optical endoscopes are Class II medical devices; they must undergo a full inspection and receive a passing record before sale. Inspection records must meet traceability requirements to quickly identify batches and causes in case of adverse events, minimizing legal risk.

Even with qualified components, assembly can introduce issues like eccentricity, optical axis shifts, or poor fiber coupling. Our finished product inspection acts as the final defense, detecting system deviations and preventing defects from entering the operating room. Endofuture’s inspection standards differ based on national regulations and industry standards. We also excel at assisting partners in establishing their own Final inspection protocols to ensure every unit shipped is flawless.