Last synced on 14 November 2025 at 11:06 pm

InMode Diolaze XL

Page Type
Cleared 510(K)
510(k) Number
K170738
510(k) Type
Traditional
Applicant
InMode MD Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/7/2017
Days to Decision
150 days
Submission Type
Summary

InMode Diolaze XL

Page Type
Cleared 510(K)
510(k) Number
K170738
510(k) Type
Traditional
Applicant
InMode MD Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/7/2017
Days to Decision
150 days
Submission Type
Summary