Aribex, Inc. is one of 18984 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aribex, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NOMAD MD 75K V HANDHELD X-RAY SYSTEM, NOMAD PRO X-RAY SYSTEM, NOMAD DENTAL X-RAY SYSTEM
3
Total
3
Cleared
0
Denied
Aribex, Inc. has 3 FDA 510(k) cleared medical devices. Based in Orem, US.
Historical record: 3 cleared submissions from 2005 to 2014. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Aribex, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Aribex, Inc.
3 devices