Last synced on 14 November 2025 at 11:06 pm

Night Guard

Page Type
Cleared 510(K)
510(k) Number
K202465
510(k) Type
Traditional
Applicant
3D Diagnostix Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/2020
Days to Decision
90 days
Submission Type
Summary

Night Guard

Page Type
Cleared 510(K)
510(k) Number
K202465
510(k) Type
Traditional
Applicant
3D Diagnostix Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/2020
Days to Decision
90 days
Submission Type
Summary