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.

2 devices

1–2 of 2