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AEON-C™ Stand Alone System

Page Type
Cleared 510(K)
510(k) Number
K223140
510(k) Type
Traditional
Applicant
Dio Medical Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2022
Days to Decision
77 days
Submission Type
Summary

AEON-C™ Stand Alone System

Page Type
Cleared 510(K)
510(k) Number
K223140
510(k) Type
Traditional
Applicant
Dio Medical Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2022
Days to Decision
77 days
Submission Type
Summary