Sunstar Americas, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sunstar Americas, Inc. - FDA 510(k) Cleared Devices
Recent clearances: G•U•M HYDRAL Dry Mouth Oral Gel, G•U•M HYDRAL Dry Mouth Oral Rinse, G•U•M HYDRAL Dry Mouth Oral Spray
3
Total
3
Cleared
0
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