Fuji Dynamics , Ltd. is one of 1430 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Fuji Dynamics , Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Fuji Dynamics , Ltd. has 5 FDA 510(k) cleared medical devices. Based in Hong Kong, CN.
Historical record: 5 cleared submissions from 2011 to 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Fuji Dynamics , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Fuji Dynamics , Ltd.
5 devices
Cleared
Jul 12, 2016
Fuji Dynamics Incontinence Stimulation Electrode, Models Fuji – 01/ 02/ 03/...
Gastroenterology & Urology
89d
Cleared
Jan 22, 2016
FD TENS 2090, FD TENS 2095
Neurology
126d
Cleared
Jan 13, 2016
LL TENS 160A, LL TENS 160B
Neurology
145d
Cleared
Mar 01, 2012
FD TENS 2070
Neurology
262d
Cleared
Nov 09, 2011
FD TENS 2050 OR SLIDE TENS MODEL FD2050
Neurology
149d