Last synced on 25 January 2026 at 3:41 am

reVive Perioral

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172662
510(k) Type
Traditional
Applicant
Led Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2018
Days to Decision
126 days
Submission Type
Summary

reVive Perioral

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172662
510(k) Type
Traditional
Applicant
Led Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2018
Days to Decision
126 days
Submission Type
Summary