Aggregates FDA MAUDE device adverse event reports (openFDA /device/event) into summary rows by product code, manufacturer, or brand -- event-type counts, top device/patient problems, monthly trend, and report-source breakdown. No individual report rows or narratives.
Every new FDA 510(k), PMA, and De Novo clearance plus device recalls, enforcement actions, and establishment registrations for your product codes or companies, with weekly diff mode. Clean rows, summary links.
Medicare physician, clinical lab, and DMEPOS fee schedules by CPT/HCPCS and locality, with LCD coverage matches and office vs ASC vs hospital comparisons. Built on current CMS files, verified to the cent.
Allowed amount, Medicare payment, patient coinsurance, sequestration, and modifier effects for any CPT by locality and site of service. Built on current CMS fee schedule files.