Terumo Corp. is one of 11743 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Terumo Corp. - FDA 510(k) Cleared Devices
Recent clearances: TERUMO SURSHIELD- PUR SAFETY I.V. CATHETER, HEARTRAIL III GUIDING CATHETER, SINGLE USE GUIDEWIRE, MODELS G-240-2527S, G-240-2545S, G-240-2527A, G-240-2545A, G-240-3527S, G-240-3545S & G-240-3527A
21
Total
21
Cleared
0
Denied
Terumo Corp. has 21 FDA 510(k) cleared medical devices. Based in Somerset, US.
Historical record: 21 cleared submissions from 1991 to 2010. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Terumo Corp. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Technology Services, LLC and Kema Quality B.V..
FDA 510(k) Regulatory Record - Terumo Corp.
21 devices
Cleared
Feb 26, 2010
TERUMO SURSHIELD- PUR SAFETY I.V. CATHETER
General Hospital
25d
Cleared
Sep 11, 2009
HEARTRAIL III GUIDING CATHETER
Cardiovascular
37d
Cleared
May 22, 2009
SINGLE USE GUIDEWIRE, MODELS G-240-2527S, G-240-2545S, G-240-2527A,...
Gastroenterology & Urology
9d
Cleared
May 01, 2009
TERUMO SURSHIELD SAFETY I.V. CATHETER (18G X 51MM & 20G X 51MM SIZES)
General Hospital
25d
Cleared
Mar 05, 2008
CAPIOX CIRCUIT CONNECTORS
Cardiovascular
85d
Cleared
Jul 23, 2007
CAPIOX FX05 HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER
Cardiovascular
45d
Cleared
Jul 16, 2007
CAPIOX FX15 AND FX25 HOLLOW FIBER OXYGENATOR AND ARTERIAL FILTER
Cardiovascular
47d
Cleared
May 25, 2007
TERUMO DIGITAL BLOOD PRESSURE MONITOR ES-H55A
Cardiovascular
39d
Cleared
Oct 13, 2004
FOUNDATION
Dental
201d
Cleared
Mar 03, 2004
CAPIOX RX25 HOLLOW FIBER OXYGENATOR W/WO HARDSHELL RESERVOIR
Cardiovascular
33d
Cleared
Dec 11, 2003
GLIDESHEATH
Cardiovascular
17d
Cleared
May 30, 2003
SURSHIELD SAFETY WINGED INFUSION SET
General Hospital
39d