Omnisonics Medical Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Omnisonics Medical Technologies - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Omnisonics Medical Technologies has 8 FDA 510(k) cleared medical devices. Based in Wilmington, US.
Historical record: 8 cleared submissions from 1999 to 2008. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Omnisonics Medical Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Omnisonics Medical Technologies
8 devices
Cleared
Dec 15, 2008
MODIFIED OMNIWAVE ENDOVASCULAR SYSTEM
Cardiovascular
33d
Cleared
Sep 27, 2007
OMNIWAVE ENDOVASCULAR SYSTEM
Cardiovascular
90d
Cleared
Dec 08, 2005
RESOLUTION ENDOVASCULAR SYSTEM
Cardiovascular
97d
Cleared
Sep 01, 2004
RESOLUTION THROMBECTOMY SYSTEM, MODEL EV-2
Cardiovascular
70d
Cleared
Mar 08, 2001
OMNISONICS ULTRASONIC SURGERY SYSTEM, MODEL STI
General & Plastic Surgery
87d
Cleared
Dec 15, 1999
OMNISONICS ULTRASONIC PROBES
General & Plastic Surgery
49d
Cleared
Dec 06, 1999
OMNISONIC ENDOSCOPIC DEFLECTOR
Gastroenterology & Urology
55d
Cleared
Jul 12, 1999
OMNISONICS FLEXIBLE FIBER OPTIC ENDOSCOPE AND COUPLER
General & Plastic Surgery
82d