Last synced on 14 November 2025 at 11:06 pm

Difiney Anti Snoring Device

Page Type
Cleared 510(K)
510(k) Number
K233850
510(k) Type
Traditional
Applicant
Fissiontech, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2024
Days to Decision
135 days
Submission Type
Summary

Difiney Anti Snoring Device

Page Type
Cleared 510(K)
510(k) Number
K233850
510(k) Type
Traditional
Applicant
Fissiontech, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2024
Days to Decision
135 days
Submission Type
Summary