Medical Device Manufacturer · US , Elk Grove Village , IL

Sunnex, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1985

Total

Cleared

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: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Sunnex, Inc. Filter by specialty or product code using the sidebar.

Sunnex, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Sunnex, Inc.

2 devices

1-2 of 2