Oroscience, Inc. is one of 21679 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oroscience, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PERIOGENIX, CURATIVE980 DIODE LASER
2
Total
2
Cleared
0
Denied
Oroscience, Inc. has 2 FDA 510(k) cleared medical devices. Based in Palo Alto, US.
Historical record: 2 cleared submissions from 2008 to 2009. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Oroscience, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Oroscience, Inc.
2 devices