Dio Medical Co., Ltd.
Dio Medical Co., Ltd. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 16, 2017.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Known Names
dio medical, dio medical co
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K162849 | Huvex Interspinous Fixation System | February 16, 2017 |
| K162220 | DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) Cage | November 21, 2016 |
| K122872 | INTERVERTEBRAL BODY FUSION DEVICE | February 28, 2013 |
| K121862 | REX ANTERIOR CERVICAL PLATE SYSTEM | October 31, 2012 |
| K113324 | REXIOUS HOOK FIXATION SYSTEMS | March 28, 2012 |
| K111362 | REXIOUS SPINAL FIXATION SYSTEM | July 21, 2011 |
| K100765 | FIXPINE II SYSTEM | July 19, 2010 |