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/ Aiomega, LLC
Aiomega, LLC
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K252525
AIO Breathe
November 6, 2025
K233754
AIO Breathe
February 23, 2024