Sorin Group Deutschland GmbH is one of 13113 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sorin Group Deutschland GmbH - FDA 510(k) Cleared Devices
Recent clearances: Sorin Connect, XTRA, SORIN FLEXTHERM
20
Total
20
Cleared
0
Denied
Sorin Group Deutschland GmbH has 20 FDA 510(k) cleared cardiovascular devices. Based in North Attleboro, US.
Historical record: 20 cleared submissions from 2006 to 2017.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Tuv Sud America, Inc. and Sorin Group USA, Inc..
FDA 510(k) Regulatory Record - Sorin Group Deutschland GmbH
20 devices
Cleared
Jun 08, 2017
Sorin Connect
Cardiovascular
113d
Cleared
Mar 21, 2014
XTRA
Anesthesiology
295d
Cleared
Jan 31, 2014
SORIN FLEXTHERM
Cardiovascular
29d
Cleared
Jul 23, 2013
SORIN CONNECT DATA MANAGEMENT SYSTEM
Cardiovascular
33d
Cleared
Sep 20, 2011
SORIN CENTRIFUGAL PUMP 5 (CP5)
Cardiovascular
48d
Cleared
Jan 20, 2011
STOCKERT CENTRIFUGAL PUMP (SCP PLUS) (COMPLETE) OR (FOR S5/C5 SYSTEMS)
Cardiovascular
57d
Cleared
Jan 20, 2011
SORIN C5 SYSTEM
Cardiovascular
28d
Cleared
Jan 18, 2011
STOCKERT AIR PURGE CONTROL SYSTEM MODEL 23-45-05
Cardiovascular
55d
Cleared
Jan 06, 2011
B-CARE5 (B-CARE5 SENSOR MODULE, VENOUS SENSOR, HOLDER FOR MEASURING HEAD)
Cardiovascular
71d
Cleared
Dec 09, 2010
STOCKERT S5 SYSTEM AND GAS BLENDER AND SORIN C5 SYSTEM
Cardiovascular
239d
Cleared
Jan 15, 2010
SORIN C5 SYSTEM MODEL 58-00-00
Cardiovascular
28d
Cleared
Nov 05, 2009
SORIN B-CARE5 FOR THE STOCKERT S5 SYSTEM
Cardiovascular
86d