Uni-Patch, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Uni-Patch, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Uni-Patch, Inc. has 6 FDA 510(k) cleared medical devices. Based in Wabasha, US.
Historical record: 6 cleared submissions from 1987 to 1999. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Uni-Patch, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Uni-Patch, Inc.
6 devices
Cleared
Sep 17, 1999
TENS/FES/NMES ELECTRODES
Neurology
389d
Cleared
Sep 05, 1996
SPEC T.E.N.S. PREWIRED REPOSITIONABLE TENS ELECTRODE - MODIFY
Neurology
62d
Cleared
Jul 31, 1996
TENS/FES/NMES ELECTRODES
Neurology
44d
Cleared
May 10, 1996
EASY FLEX TENS/FES/MNS ELECTRODES 2 ROUND MODEL 8200/2X2 MODEL 8220
Neurology
50d
Cleared
Aug 26, 1993
CONDUCT ALOE GEL, #UP239-8FL. OZ/#UP245 G-1 GALLON
Neurology
301d
Cleared
May 29, 1987
TANTONE MULTI-DAY #633 TENS ELECTRODE
Neurology
63d