Medical Device Manufacturer · US , Bellevue , WA

Sagemax Bioceramics, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2006

Total

Cleared

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. is one of 5644 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Sagemax Bioceramics, Inc.

2 devices

1-2 of 2