Ld Technology, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ld Technology, LLC - FDA 510(k) Cleared Devices
Recent clearances: BP-BT Kiosk, Oxi-W System
14
Total
14
Cleared
0
Denied
Ld Technology, LLC has 14 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 14 cleared submissions from 2009 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ld Technology, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ld Technology, LLC
14 devices
Cleared
May 15, 2020
BP-BT Kiosk
Cardiovascular
100d
Cleared
Apr 27, 2020
Oxi-W System
Anesthesiology
97d
Cleared
Dec 19, 2017
TBL-ABI System
Cardiovascular
18d
Cleared
Jul 06, 2016
LD-Oxi system
Cardiovascular
92d
Cleared
Sep 24, 2015
SudoC
Neurology
48d
Cleared
Jul 22, 2015
TM-ABI system
Cardiovascular
261d
Cleared
May 22, 2014
ANS1 SOFTWARE
Cardiovascular
93d
Cleared
Jun 28, 2013
SUDO PATH
Neurology
29d
Cleared
Apr 11, 2013
PATIENT MONITOR
Cardiovascular
92d
Cleared
Mar 02, 2012
ELECTRO SENSOR COMPLEX SOFTWARE (ES COMPLEX SOFTWARE)
Cardiovascular
119d
Cleared
Mar 29, 2011
ELECTRO SENSOR -BODY COMPOSITION
Gastroenterology & Urology
168d
Cleared
Dec 10, 2010
ELECTRO INTERSTITIAL SCAN
Neurology
130d
Cleared
Sep 10, 2010
E.S.O. (ELECTRO SENSOR OXI)
Anesthesiology
15d
Cleared
Feb 23, 2009
E.S TECK ( ELECTRO SENSOR TECK)
Cardiovascular
112d