Last synced on 25 January 2026 at 3:41 am

Unicorn+ RF System (Unicorn+); Unicorn+ RF System (Unicorn+ I); Unicorn+ RF System (Unicorn+ II); Unicorn+ RF System (Unicorn+ III)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241832
510(k) Type
Traditional
Applicant
Boston Aesthetics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2025
Days to Decision
233 days
Submission Type
Summary

Unicorn+ RF System (Unicorn+); Unicorn+ RF System (Unicorn+ I); Unicorn+ RF System (Unicorn+ II); Unicorn+ RF System (Unicorn+ III)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241832
510(k) Type
Traditional
Applicant
Boston Aesthetics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2025
Days to Decision
233 days
Submission Type
Summary