AI Planning Logic, Inc. is one of 12968 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
AI Planning Logic, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Lower Limb AI (LLAI)
1
Total
1
Cleared
0
Denied
AI Planning Logic, Inc. has 1 FDA 510(k) cleared medical devices. Based in Santa Rosa, US.
Latest FDA clearance: Aug 2026. Active since 2026. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by AI Planning Logic, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Sagemar Medical, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - AI Planning Logic, Inc.
1 devices