Sagemax Bioceramics, Inc. is one of 5134 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sagemax Bioceramics, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Sagemax Bioceramics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Bellevue, US.
Historical record: 2 cleared submissions from 2006 to 2014. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Sagemax Bioceramics, Inc. Filter by specialty or product code using the sidebar.
Sagemax Bioceramics, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Feb 10, 2014
NEXXZR(TM)T AND NEXXZR(TM)S
Dental
306d
Cleared
Oct 20, 2006
SAGEMAX Z-BLANK
Dental
39d