Levtech, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Levtech, Inc. has 5 FDA 510(k) cleared medical devices. Based in Jacksonville, US.
Historical record: 5 cleared submissions from 1985 to 1991. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Levtech, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Jun 18, 1991
LEVTECH TITANIUM BONE WIRE
Orthopedic
160d
Cleared
Oct 10, 1990
LEVTECH BONE SCREW
Orthopedic
212d
Cleared
Feb 05, 1988
LEVTECH COMPOSITE TRACTION TONGS
Neurology
144d
Cleared
Nov 06, 1987
LEVTECH CLAMP APPLIER
General & Plastic Surgery
35d
Cleared
May 29, 1985
HALIFAX SPINAL CLAMP
Orthopedic
142d