Last synced on 14 November 2025 at 11:06 pm

Adravision Perio

Page Type
Cleared 510(K)
510(k) Number
K232440
510(k) Type
Traditional
Applicant
Adra Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/2023
Days to Decision
113 days
Submission Type
Summary

Adravision Perio

Page Type
Cleared 510(K)
510(k) Number
K232440
510(k) Type
Traditional
Applicant
Adra Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/2023
Days to Decision
113 days
Submission Type
Summary