Tactile Systems Technology, Inc. is one of 18926 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tactile Systems Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: entré Model PD08-U, ACTITOUCH ACT-ADAPTIVE COMPRESSION THERAPY SYSTEM, FLEXITOUCH SYSTEM
5
Total
5
Cleared
0
Denied
Tactile Systems Technology, Inc. has 5 FDA 510(k) cleared medical devices. Based in Shakopee, US.
Historical record: 5 cleared submissions from 2002 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Tactile Systems Technology, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Intertek Testing Services and Underwriters Laboratories, Inc..
FDA 510(k) Regulatory Record - Tactile Systems Technology, Inc.
5 devices
Cleared
May 07, 2015
entré Model PD08-U
Cardiovascular
183d
Cleared
Jun 18, 2013
ACTITOUCH ACT-ADAPTIVE COMPRESSION THERAPY SYSTEM
Cardiovascular
53d
Cleared
Apr 13, 2012
FLEXITOUCH SYSTEM
Cardiovascular
11d
Cleared
Oct 06, 2006
FLEXITOUCH SYSTEM
Cardiovascular
16d
Cleared
Jul 01, 2002
BIOTOUCH MASSAGE THERAPY SYSTEM
Physical Medicine
293d