Dornoch Medical Systems, Inc. is one of 5129 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dornoch Medical Systems, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Dornoch Medical Systems, Inc. has 3 FDA 510(k) cleared medical devices. Based in Riverside, US.
Historical record: 3 cleared submissions from 2008 to 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Dornoch Medical Systems, Inc. Filter by specialty or product code using the sidebar.
Dornoch Medical Systems, Inc. — FDA 510(k) Products and Clearance History
3 devices
Cleared
Mar 21, 2014
DORNOCH DUO SUCTION CART WITH: DL2800 LID, CL500 LID, DORNOCH QUAD SUCTION...
General & Plastic Surgery
99d
Cleared
Mar 04, 2013
DORNOCH DUO SUCTION CART WITH DL2800 LID MODEL UL-DU2800, DORNOCH DUO SUCTION...
General & Plastic Surgery
144d
Cleared
Apr 29, 2008
TRANSPOSAL ULTRA SYSTEMS
General & Plastic Surgery
15d