US Original PMAs and Panel-Track Supplementss
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
US PMA Supplements
PMA supplements approved by US FDA’s Center for Devices and Radiological Health. 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.
Compliance
Commercial
Medtech Company Financing
Financings, M&A and alliances across the medical device, diagnostics and digital health sectors. Data derived from Citeline’s Meddevicetracker.