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Facet Aurora Reusable Lancet Base

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232912
510(k) Type
Traditional
Applicant
Facet Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2024
Days to Decision
128 days
Submission Type
Summary

Facet Aurora Reusable Lancet Base

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232912
510(k) Type
Traditional
Applicant
Facet Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2024
Days to Decision
128 days
Submission Type
Summary