US Original PMAs and Panel-Track Supplements
Class III devices and panel-track supplements approved by US FDA’s Center for Devices and Radiological Health. Data derived from FDA.gov. Updated weekly.
Medtech Insight Data Trackers
Keep tabs on device approvals in the US and abroad, US Breakthrough Device designations, warning letters, guidances, M&A and more.
Approvals
Non-US Approvals
Devices authorized for marketing outside the US. Data derived from Citeline’s Meddevicetracker. Updated weekly.