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Altaviz, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243322Altaviz Intravitreal SyringeMay 9, 2025
K231261Altaviz Needle Kit IIJuly 27, 2023
K222681Altaviz Needle KitDecember 5, 2022