Acucera, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Acucera, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Acucera, Inc. has 2 FDA 510(k) cleared medical devices. Based in Seul, KR.
Historical record: 2 cleared submissions from 2005 to 2007. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Acucera, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Acucera, Inc.
2 devices