Medical Device Manufacturer · US , Lake Bluff , IL

Sunstar Americas, Inc.

3 submissions · 3 cleared · Since 2011
3
Total
3
Cleared
0
Denied

Sunstar Americas, Inc. — FDA 510(k) Submissions

Sunstar Americas, Inc. has submitted 3 FDA 510(k) premarket notifications since 2011, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Saliva, Artificial, Agent, Polishing, Abrasive, Oral Cavity, Barrier, Synthetic, Intraoral . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
Filters
Filter by Specialty
All3 Dental 3