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FDA 510(k) Applications Submitted by Leonid Lerner
FDA 510(k) Number
Submission Date
Device Name
Applicant
K230372
02/13/2023
VitreJect Syringe
OcuJect, LLC
K230959
04/04/2023
VitreJect« Needle; OcuSafe« Needle
OcuJect, LLC
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