Sunnex, Inc. is one of 14540 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sunnex, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Leo Minor
2
Total
2
Cleared
0
Denied
Sunnex, Inc. has 2 FDA 510(k) cleared medical devices. Based in Elk Grove Village, US.
Historical record: 2 cleared submissions from 1985 to 2014. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Sunnex, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Sunnex, Inc.
2 devices