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Fraxel® FTX Laser System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242142
510(k) Type
Traditional
Applicant
Solta Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2024
Days to Decision
30 days
Submission Type
Statement

Fraxel® FTX Laser System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242142
510(k) Type
Traditional
Applicant
Solta Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2024
Days to Decision
30 days
Submission Type
Statement