Last synced on 14 November 2025 at 11:06 pm

truSculpt iD

Page Type
Cleared 510(K)
510(k) Number
K221407
510(k) Type
Traditional
Applicant
Cutera, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2022
Days to Decision
58 days
Submission Type
Summary

truSculpt iD

Page Type
Cleared 510(K)
510(k) Number
K221407
510(k) Type
Traditional
Applicant
Cutera, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2022
Days to Decision
58 days
Submission Type
Summary