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
K242956 09/25/2024 LDS Needle; OcuSafe« LDS Needle; SteriCap« LDS Safety Needle; VitreJect« LDS Safety Needle OcuJect, LLC
K233343 09/29/2023 SteriCap Safety Needle; VitreJect Safety Needle OcuJect, LLC


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact