Vestil Manufacturing Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vestil Manufacturing Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Vestil Manufacturing Corp. has 6 FDA 510(k) cleared medical devices. Based in Angola, US.
Historical record: 6 cleared submissions from 2000 to 2009. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Vestil Manufacturing Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vestil Manufacturing Corp.
6 devices
Cleared
Apr 10, 2009
EXTREME 4X4-X8 POWER WHEELCHAIR
Physical Medicine
58d
Cleared
Apr 04, 2003
FRONTIER MODEL X5
Physical Medicine
23d
Cleared
Jun 14, 2002
KARMA 800 SERIES MANUAL WHEELCHAIR
Physical Medicine
8d
Cleared
Mar 15, 2002
KARMA DISCOVERY, MODEL KP40
Physical Medicine
88d
Cleared
May 29, 2001
JEWEL MPS
Physical Medicine
25d
Cleared
Aug 11, 2000
MAGIC MOBILITY 4 X 4 WHEELCHAIR
Physical Medicine
151d