JMS North America Corporation - FDA 510(k) Cleared Devices

JMS North America Corporation has 9 FDA 510(k) cleared medical devices. Based in Crofton, US.

Latest FDA clearance: Aug 2025. Active since 2011. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by JMS North America Corporation Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Smith Assoicates as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.