Kent Design & Manufacturing, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kent Design & Manufacturing, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Kent Design & Manufacturing, Inc. has 6 FDA 510(k) cleared medical devices. Based in Grand Rapids, US.
Historical record: 6 cleared submissions from 1986 to 1986. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Kent Design & Manufacturing, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kent Design & Manufacturing, Inc.
6 devices
Cleared
Aug 20, 1986
PORTABLE ISOKINETICS 3001 WRIST/ANKLE UNIT
Physical Medicine
12d
Cleared
Aug 20, 1986
PORTABLE ISOKINETICS 3002 ISO KANE II
Physical Medicine
12d
Cleared
Aug 20, 1986
PORTABLE ISOKINETICS 3003 SHOULDER UNIT
Physical Medicine
12d
Cleared
Aug 20, 1986
PORTABLE ISOKINETICS 3004 KNEE UNIT
Physical Medicine
12d
Cleared
Aug 20, 1986
PORTABLE ISOKINETICS 3005 HIP UNIT
Physical Medicine
12d
Cleared
Aug 20, 1986
PORTABLE ISOKINETICS 3007 BACK/ABDOMEN UNIT
Physical Medicine
12d