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Venus BlissMAX

Page Type
Cleared 510(K)
510(k) Number
K213308
510(k) Type
Traditional
Applicant
Venus Concept USA Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2022
Days to Decision
100 days
Submission Type
Summary

Venus BlissMAX

Page Type
Cleared 510(K)
510(k) Number
K213308
510(k) Type
Traditional
Applicant
Venus Concept USA Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2022
Days to Decision
100 days
Submission Type
Summary