Dio Medical Corp.

FDA Regulatory Profile

Dio Medical Corp. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 9, 2023.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Known Names

dio medical, dio medical co

Recent 510(k) Clearances

K-NumberDeviceDate
K223790Huvex Interspinous Fusion SystemMarch 9, 2023
K223140AEON-C™ Stand Alone SystemDecember 20, 2022