Tempus AI
Organization · Company · US · 2 items since Aug 2026
Deals & regulation
- Sep 28
Cleared by U.S. Food and Drug Administration
- Aug 24
Cleared by U.S. Food and Drug Administration
Models & products
- Products
Items
- Sep 28
FDA clears Tempus ECG-MR
The FDA granted 510(k) clearance to an AI product that analyzes standard 12-lead ECGs to flag signs of undiagnosed moderate or severe mitral regurgitation in at-risk patients 65 and older, as an early-detection referral tool.
- Aug 24
FDA clears Tempus ECG-PH
The FDA cleared AI software that reads standard 12-lead ECGs for signs of pulmonary hypertension, an assistive binary readout aimed at earlier detection of a historically underdiagnosed condition and Tempus's third cleared cardiovascular device.