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
US PMA Supplements
PMA supplements approved by US FDA’s Center for Devices and Radiological Health. Data derived from FDA.gov. Updated weekly.
US 510(k) Clearances
Devices cleared for market via US FDA’s 510(k) pathway. Data derived from FDA.gov. Updated weekly.
US De Novo Classifications
Devices granted De Novo marketing authorization by the US FDA. Data derived from FDA.gov Updated weekly.
Non-US Approvals
Devices authorized for marketing outside the US. Data derived from Citeline’s Meddevicetracker. Updated weekly.