Last synced on 14 November 2025 at 11:06 pm

Ivotion Base Print

Page Type
Cleared 510(K)
510(k) Number
K233995
510(k) Type
Traditional
Applicant
Ivoclar Vivadent, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2024
Days to Decision
67 days
Submission Type
Summary

Ivotion Base Print

Page Type
Cleared 510(K)
510(k) Number
K233995
510(k) Type
Traditional
Applicant
Ivoclar Vivadent, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2024
Days to Decision
67 days
Submission Type
Summary