Last synced on 12 July 2024 at 11:04 pm

EK Digital Abutments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233389
510(k) Type
Traditional
Applicant
Hiossen, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/2024
Days to Decision
240 days
Submission Type
Summary

EK Digital Abutments

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233389
510(k) Type
Traditional
Applicant
Hiossen, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/2024
Days to Decision
240 days
Submission Type
Summary