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ETIII SA Fixture System (O3.2mm)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153332
510(k) Type
Traditional
Applicant
Hiossen, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2016
Days to Decision
343 days
Submission Type
Summary

ETIII SA Fixture System (O3.2mm)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153332
510(k) Type
Traditional
Applicant
Hiossen, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/27/2016
Days to Decision
343 days
Submission Type
Summary