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UV Active Implant System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182194
510(k) Type
Traditional
Applicant
DIO Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
12/14/2018
Days to Decision
122 days
Submission Type
Summary

UV Active Implant System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182194
510(k) Type
Traditional
Applicant
DIO Corporation
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
12/14/2018
Days to Decision
122 days
Submission Type
Summary