510(k) K252525

Device
AIO Breathe
Applicant
Aiomega, LLC
510(k) number
K252525
Product code
LRK
Decision
Substantially Equivalent (SESE)
Decision date
2025-11-06
Date received
2025-08-11
Regulation
872.5570
Classification name
Device, Anti-Snoring
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Abbreviated
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Raghavendra Ghuge
Address
3187 Paluxy Dr. Tyler TX US 75701 75701

FDA Registration Numbers

Source Documents

510(k) summary PDF

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