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Diality, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K243607Moda-flx Hemodialysis System™ Cartridge (102121-001 )December 20, 2024
K233798Moda-flx Hemodialysis System and CartridgeAugust 2, 2024