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Ulthera System (UC-1 Control Unit PRIME Model 2.1)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250418
510(k) Type
Traditional
Applicant
Ulthera Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2025
Days to Decision
89 days
Submission Type
Summary

Ulthera System (UC-1 Control Unit PRIME Model 2.1)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250418
510(k) Type
Traditional
Applicant
Ulthera Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2025
Days to Decision
89 days
Submission Type
Summary