Affirm Medical Technologies II, LLC is one of 16340 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Affirm Medical Technologies II, LLC - FDA 510(k) Cleared Devices
Recent clearances: VisuBreath
1
Total
1
Cleared
0
Denied
Affirm Medical Technologies II, LLC has 1 FDA 510(k) cleared medical devices. Based in Piedmont, US.
Latest FDA clearance: Jul 2026. Active since 2026. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Affirm Medical Technologies II, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Jenelle N. Mohan, Esq as regulatory consultant.
FDA 510(k) Regulatory Record - Affirm Medical Technologies II, LLC
1 devices