Dixi Medical

FDA Regulatory Profile

Dixi Medical appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 18, 2021.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K202087DIXI Medical Microdeep Micro-Macro Depth ElectrodesNovember 18, 2021
K201931Dixi Medical Intraoperative Subdural Electrodes (Strips and Grids)October 2, 2021
K170959DIXI Medical Microdeep Depth ElectrodeNovember 24, 2017