FDA applicant
Medimop Medical Projects, Ltd.
FDA records 12 decisions for Medimop Medical Projects, Ltd. (Ra'Anana, IL) from 1996 to 2016: 12 510(k) clearances. Most are in product codes LHI (Set, I.V. Fluid Transfer) and FMF (Syringe, Piston). Its devices cite 21 predicates, 12 of them its own earlier devices. 2 recalls are linked to its devices, 1 Class I.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Medimop Medical Projects, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2016
2026 so far, outlined.
Recalls per year
1in 2018
Class I Class II/III not classified
Planning a device like Medimop Medical Projects, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Medimop”
FDA records each applicant name separately; these may or may not be the same firm.