Altaviz, LLC

FDA Regulatory Profile

Altaviz, LLC appears in FDA public data with 0 recalls, 3 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 9, 2025.

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