FDA AI Clearance Tracker/K253825

Radiology · 510(k)

Saige-Dx

DeepHealth, Inc.

Device
Saige-Dx
Company
DeepHealth, Inc.
Submission number
K253825
Pathway
510(k)
Decision date
Jun 15, 2026
Specialty (lead panel)
Radiology
Primary product code
QDQ

Source: U.S. FDA AI-Enabled Medical Devices list. The FDA says the list is not comprehensive. Confirm details on the FDA's own record.