Last synced on 9 May 2025 at 11:05 pm

Endofill

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231387
510(k) Type
Traditional
Applicant
Lumendo AG
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
7/10/2023
Days to Decision
59 days
Submission Type
Summary

Endofill

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231387
510(k) Type
Traditional
Applicant
Lumendo AG
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
7/10/2023
Days to Decision
59 days
Submission Type
Summary