Dio Medical Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K162849Huvex Interspinous Fixation SystemFebruary 16, 2017
K162220DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) CageNovember 21, 2016
K122872INTERVERTEBRAL BODY FUSION DEVICEFebruary 28, 2013
K121862REX ANTERIOR CERVICAL PLATE SYSTEMOctober 31, 2012
K113324REXIOUS HOOK FIXATION SYSTEMSMarch 28, 2012
K111362REXIOUS SPINAL FIXATION SYSTEMJuly 21, 2011
K100765FIXPINE II SYSTEMJuly 19, 2010