Texasmedical Technologies, Inc. is one of 18410 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Texasmedical Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TXM Support Catheter, TXM Hydrophilic Guidewire, TXM Guiding Sheath
7
Total
7
Cleared
0
Denied
Texasmedical Technologies, Inc. has 7 FDA 510(k) cleared medical devices. Based in El Paso, US.
Historical record: 7 cleared submissions from 2015 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Texasmedical Technologies, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Smith Associates and Pomamed Consulting, LLC.
FDA 510(k) Regulatory Record - Texasmedical Technologies, Inc.
7 devices
Cleared
Nov 21, 2017
TXM Support Catheter
Cardiovascular
238d
Cleared
Nov 21, 2017
TXM Hydrophilic Guidewire
Cardiovascular
238d
Cleared
Sep 13, 2016
TXM Guiding Sheath
Cardiovascular
258d
Cleared
May 12, 2016
Guiding Catheter
Cardiovascular
141d
Cleared
Jan 13, 2016
IntraNovo Microcatheter
Cardiovascular
76d
Cleared
May 28, 2015
PTA 14 Balloon Dilatation Catheter OTW
Cardiovascular
230d
Cleared
Apr 23, 2015
IntraNovo 25 Microcatheter
Cardiovascular
206d