510(k) Report

FDA applicant

Mediziv Medical Devices, Ltd.

Israel, IL2 decisions1989–19890 recalls

FDA records 2 decisions for Mediziv Medical Devices, Ltd. (Israel, IL) in 1989: 2 510(k) clearances. Most are in product codes CAZ (Anesthesia Conduction Kit) and DQY (Catheter, Percutaneous). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, anesthesiology panel, where it files most

How often FDA has decided Mediziv Medical Devices, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mediziv Medical Devices, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Mediziv Medical Devices, Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • CAZAnesthesia Conduction Kit1decision
  • DQYCatheter, Percutaneous1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K894725Mediziv Epidural SystemsMediziv Medical Devices, Ltd. · 19891cites it

What has FDA decided for it lately?

  • K894725Mediziv Epidural SystemsMediziv Medical Devices, Ltd. · 1989
  • K884491Mediziv Central Vein CatheterMediziv Medical Devices, Ltd. · 1989

All 2 as Mediziv Medical Devices, Ltd. →

Other applicant names beginning “Mediziv”

FDA records each applicant name separately; these may or may not be the same firm.

Mediziv Medical Products 1987, Ltd. 4Mediziv Medical Products, Ltd. 1