Dornoch Medical Systems, Inc. is one of 18943 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
Recent clearances: DORNOCH DUO SUCTION CART WITH: DL2800 LID, CL500 LID, DORNOCH QUAD SUCTION CART WITH: DL2800 LID, CL500 LID, DORNOCH DUO SUCTION CART WITH DL2800 LID MODEL UL-DU2800, DORNOCH DUO SUCTION CART WITH CL500 LID MODEL UL-DU500, DORNOC, TRANSPOSAL ULTRA SYSTEMS
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.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Dornoch Medical Systems, Inc.
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