Last synced on 25 January 2026 at 3:41 am

Renuvion APR Handpiece

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220970
510(k) Type
Traditional
Applicant
Apyx Medical Corporation(Formerly Bovie Medical Corporation)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2022
Days to Decision
102 days
Submission Type
Summary

Renuvion APR Handpiece

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220970
510(k) Type
Traditional
Applicant
Apyx Medical Corporation(Formerly Bovie Medical Corporation)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2022
Days to Decision
102 days
Submission Type
Summary