International Medical Devices, Inc. - FDA 510(k) Cleared Devices

International Medical Devices, Inc. has 4 FDA 510(k) cleared medical devices. Based in Beverly Hills, US.

Last cleared in 2023. Active since 2017. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by International Medical Devices, Inc. Filter by specialty or product code using the sidebar.

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