Dio Medical Corporation

Dio Medical Corporation holds 4 FDA 510(k) medical device clearances, cleared in 2022.

Top product codes for Dio Medical Corporation

Recent clearances by Dio Medical Corporation

K222415 — Rexious Spinal Fixation SystemCode NKB·2022-10-25
K222572 — FORTIS and HANA Anterior Cervical Plate System, Rex Anterior Cervical Plate System, and BALTEUM & BALTEUM-ONE Lumbar Plate SystemCode KWQ·2022-10-18
K222448 — UNITY Sacroiliac Joint Fixation SystemCode OUR·2022-10-13
K222515 — FaSet Fixation SystemCode MRW·2022-10-05

Data sourced from openFDA. This site is unofficial and independent of the FDA.