Aci, Inc. is one of 23331 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aci, Inc. - FDA 510(k) Cleared Devices
Recent clearances: GFX NERVE ABLATION SYSTEM, FLEXO DENTAL RESIN MATERIAL
2
Total
2
Cleared
0
Denied
Aci, Inc. has 2 FDA 510(k) cleared medical devices. Based in Mission, US.
Historical record: 2 cleared submissions from 2006 to 2007. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Aci, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Aci, Inc.
2 devices