Last synced on 14 November 2025 at 11:06 pm

InMode Diolaze System

Page Type
Cleared 510(K)
510(k) Number
K180719
510(k) Type
Traditional
Applicant
InMode MD Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
6/14/2018
Days to Decision
87 days
Submission Type
Summary

InMode Diolaze System

Page Type
Cleared 510(K)
510(k) Number
K180719
510(k) Type
Traditional
Applicant
InMode MD Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
6/14/2018
Days to Decision
87 days
Submission Type
Summary