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reVive Perioral

Page Type
Cleared 510(K)
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)
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