Jeil Medical Corporation - FDA 510(k) Cleared Devices
53
Total
53
Cleared
0
Denied
40 devices
Cleared
Aug 14, 2017
ARIX Foot System (2.3/2.8)
Orthopedic
152d
Cleared
Jul 27, 2017
ARIX Ankle Distal Tibia System
Orthopedic
176d
Cleared
Jul 24, 2017
ARIX Diaphysis System
Orthopedic
84d
Cleared
Dec 27, 2016
SMARTO
Orthopedic
34d
Cleared
Sep 21, 2016
ARIX Hand System
Orthopedic
89d
Cleared
Aug 02, 2016
ARIX Foot System
Orthopedic
26d
Cleared
Jan 14, 2016
ARIX Wrist System
Orthopedic
227d
Cleared
Sep 28, 2015
ARIX Ankle System
Orthopedic
56d
Cleared
Dec 18, 2013
ARIX HAND LOCKING SYSTEM
Orthopedic
96d
Cleared
Nov 04, 2013
ARIX HAND SYSTEM
Orthopedic
158d
Cleared
Sep 05, 2013
ARIX FOOT SYSTEM
Orthopedic
121d
Cleared
Dec 17, 2010
SMARTO
Orthopedic
196d
Cleared
Nov 13, 2009
LEFORTE NEUROSYSTEM BONE SCREW
Orthopedic
157d
Cleared
Apr 18, 2003
LEFORTE SYSTEM BONE SCREW
Orthopedic
193d
Cleared
Oct 25, 2002
LEFORTE SYSTEM BONE PLATE
Orthopedic
18d