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EK Implants and Abutments System

Page Type
Cleared 510(K)
510(k) Number
K203360
510(k) Type
Traditional
Applicant
Hiossen, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2022
Days to Decision
417 days
Submission Type
Summary

EK Implants and Abutments System

Page Type
Cleared 510(K)
510(k) Number
K203360
510(k) Type
Traditional
Applicant
Hiossen, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2022
Days to Decision
417 days
Submission Type
Summary