Dio Medical Co., Ltd. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Dio Medical Co., Ltd. has 7 FDA 510(k) cleared medical devices. Based in Santa Fe Springs, US.
Historical record: 7 cleared submissions from 2010 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Dio Medical Co., Ltd. Filter by specialty or product code using the sidebar.
7 devices
Cleared
Feb 16, 2017
Huvex Interspinous Fixation System
Orthopedic
128d
Cleared
Nov 21, 2016
DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) Cage
Orthopedic
105d
Cleared
Feb 28, 2013
INTERVERTEBRAL BODY FUSION DEVICE
Orthopedic
162d
Cleared
Oct 31, 2012
REX ANTERIOR CERVICAL PLATE SYSTEM
Orthopedic
127d
Cleared
Mar 28, 2012
REXIOUS HOOK FIXATION SYSTEMS
Orthopedic
139d
Cleared
Jul 21, 2011
REXIOUS SPINAL FIXATION SYSTEM
Orthopedic
66d
Cleared
Jul 19, 2010
FIXPINE II SYSTEM
Orthopedic
124d