Qserve America, Inc. is one of 5157 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Qserve America, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Qserve America, Inc. has 2 FDA 510(k) cleared medical devices. Based in Claremont, US.
Historical record: 2 cleared submissions from 2011 to 2013. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Qserve America, Inc. Filter by specialty or product code using the sidebar.
Qserve America, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Nov 01, 2013
CLEARPATH ALIGNER
Dental
352d
Cleared
Nov 04, 2011
MEDISIZE RED AND MEDISIZE BLUE
General Hospital
281d