Dio Medical Co., Ltd.
Dio Medical Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2017.
Top product codes for Dio Medical Co., Ltd.
Recent clearances by Dio Medical Co., Ltd.
- K162849 — Huvex Interspinous Fixation System
- K162220 — DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) Cage
- K122872 — INTERVERTEBRAL BODY FUSION DEVICE
- K121862 — REX ANTERIOR CERVICAL PLATE SYSTEM
- K113324 — REXIOUS HOOK FIXATION SYSTEMS
- K111362 — REXIOUS SPINAL FIXATION SYSTEM
- K100765 — FIXPINE II SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.