Fziomed, Inc.

FDA Regulatory Profile

Fziomed, Inc. appears in FDA public data with 0 recalls, 2 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 1, 2026.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K253326OxiplexMay 1, 2026
DEN240038Oxiplex®Jun 17, 2025