Ansella Therapeutics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ansella Therapeutics - FDA 510(k) Cleared Devices
Recent clearances: Cerynë Intimate Care
1
Total
1
Cleared
0
Denied
Ansella Therapeutics has 1 FDA 510(k) cleared medical devices. Based in Cypress, US.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Ansella Therapeutics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ansella Therapeutics
1 devices