Aribex Inc

FDA Regulatory Profile

Summary

Total Recalls
2
510(k) Clearances
4
Inspections
1
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-2717-2016Class IINOMAD Pro2 Packaged X-Ray System, Part Number 08500021; NOMAD Pro2 Packaged X-Ray System Black, PartJuly 18, 2016
Z-2716-2016Class IINOMAD Pro Packaged X-Ray System, Part Number 08500009; NOMAD Pro Vet Packaged X-Ray System, Part NumJuly 18, 2016

Recent 510(k) Clearances

K-NumberDeviceDate
K173319KaVo NOMAD Pro 2 Handheld X-ray SystemNovember 16, 2017
K140723NOMAD MD 75K V HANDHELD X-RAY SYSTEMAugust 19, 2014
K081664NOMAD PRO X-RAY SYSTEMJune 23, 2008
K051795NOMAD DENTAL X-RAY SYSTEMJuly 14, 2005