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.
Compliance
Global Medtech Guidance Tracker
Comprehensively tracks regulatory guidance documents issued by medtech authorities worldwide. Updated monthly.
Commercial
Mergers and Acquisitions
Mergers and acquisitions in the medical device, diagnostics and digital health sectors. Data derived from Citeline’s Meddevicetracker.