Annalise-Ai is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Annalise-Ai - FDA 510(k) Cleared Devices
Recent clearances: Annalise Enterprise, Annalise Enterprise CXR Triage Pneumothorax
2
Total
2
Cleared
0
Denied
Annalise-Ai has 2 FDA 510(k) cleared medical devices. Based in Sydney, AU.
Latest FDA clearance: Apr 2025. Active since 2022. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Annalise-Ai Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Annalise-Ai
2 devices