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 510(k) Clearances
Devices cleared for market via US FDA’s 510(k) pathway. Data derived from FDA.gov. Updated weekly.
Compliance
Commercial
Mergers and Acquisitions
Mergers and acquisitions in the medical device, diagnostics and digital health sectors. Data derived from Citeline’s Meddevicetracker.