Jace Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Jace Systems, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Jace Systems, Inc. has 6 FDA 510(k) cleared medical devices. Based in Moorestown, US.
Historical record: 6 cleared submissions from 1992 to 1994. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Jace Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jace Systems, Inc.
6 devices
Cleared
Jun 22, 1994
JACE MODEL H440 HAND CPM DEVICE
Physical Medicine
481d
Cleared
Jun 22, 1994
ARTROMOT-E, ELBOW / ARTROMOT-S, SHOULDER CMP MOD.
Physical Medicine
365d
Cleared
Oct 08, 1993
JACE TRI-STIM DEVICE
Physical Medicine
182d
Cleared
Jun 11, 1992
JACE KNEE EXTENSION SYSTEM -- MODIFICATION
Physical Medicine
35d
Cleared
May 04, 1992
JACE MODEL PM-410 HAND CPM DEVICE
Physical Medicine
46d
Cleared
Feb 11, 1992
JACE MODEL W550 WRIST CPM DEVICE
Physical Medicine
13d