Scieran Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Scieran Technologies, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Scieran Technologies, Inc. has 5 FDA 510(k) cleared medical devices. Based in Laguna Hills, US.
Historical record: 5 cleared submissions from 1996 to 1998. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Scieran Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Scieran Technologies, Inc.
5 devices