Thought Technology , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Thought Technology , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: MyOnyx System, MyOnyx System
22
Total
22
Cleared
0
Denied
Thought Technology , Ltd. has 22 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Last cleared in 2022. Active since 1981. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Thought Technology , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Thought Technology , Ltd.
22 devices
Cleared
Jun 17, 2022
MyOnyx System
Physical Medicine
261d
Cleared
Jan 13, 2021
MyOnyx System
Gastroenterology & Urology
271d
Cleared
Mar 15, 2006
MYOTRAC INFINITI ELECTRICAL STIMULATOR
Gastroenterology & Urology
96d
Cleared
Dec 29, 2005
MYOTRAC INFINITI
Physical Medicine
36d
Cleared
Sep 29, 1995
MYOTRAC2D/CS
Gastroenterology & Urology
1081d
Cleared
May 11, 1995
THOUGHT TECHNOLOGY VAGINAL & RECTAL ELECTRODE
Gastroenterology & Urology
737d
Cleared
May 11, 1995
INCONTROL
Gastroenterology & Urology
559d
Cleared
Sep 09, 1992
MYOTRAC2
Neurology
257d
Cleared
Sep 09, 1992
MYOTRAC/S, MYODAC/S
Neurology
257d
Cleared
Mar 26, 1992
MYOTRAC+/S, MYODAC+/S
Neurology
209d
Cleared
Feb 12, 1991
FLEXCOMP DSP & PROCOMP
Neurology
193d
Cleared
Oct 09, 1990
M(3):MICRO MUSCLE MONITOR
Neurology
336d