Dio Medical Co., Ltd.
7 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| Huvex Interspinous Fixation System (K162849) | Dio Medical Co., Ltd. | 2017-02-16 |
| DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) Cage (K162220) | Dio Medical Co., Ltd. | 2016-11-21 |
| INTERVERTEBRAL BODY FUSION DEVICE (K122872) | Dio Medical Co., Ltd. | 2013-02-28 |
| REX ANTERIOR CERVICAL PLATE SYSTEM (K121862) | Dio Medical Co., Ltd. | 2012-10-31 |
| REXIOUS HOOK FIXATION SYSTEMS (K113324) | Dio Medical Co., Ltd. | 2012-03-28 |
| REXIOUS SPINAL FIXATION SYSTEM (K111362) | Dio Medical Co., Ltd. | 2011-07-21 |
| FIXPINE II SYSTEM (K100765) | Dio Medical Co., Ltd. | 2010-07-19 |
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Every clearance here is in the API, with alerts when new ones post.