Medical Device Manufacturer · US , Lake Bluff , IL

Sunstar Americas, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2011

Total

Cleared

Denied

Sunstar Americas, Inc. has 3 FDA 510(k) cleared medical devices. Based in Lake Bluff, US.

Historical record: 3 cleared submissions from 2011 to 2018. Primary specialty: Dental.

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

FDA 510(k) Regulatory Record - Sunstar Americas, Inc.

3 devices

1-3 of 3