510(k) Report

FDA applicant

Clew Medical, Ltd.

Netanya, IL2 decisions2021–20240 recalls

FDA records 2 decisions for Clew Medical, Ltd. (Netanya, IL) from 2021 to 2024: 2 510(k) clearances. All are in product code QNL (Medium-Term Adjunctive Predictive…). Its devices cite 4 predicates, 1 of them its own earlier devices. 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, cardiovascular panel, where it files most

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

FDA decisions per year

1in 2024

2021: 12024: 1
2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Clew Medical, Ltd. by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • QNLMedium-Term Adjunctive Predictive Cardiovascular Indicator2decisions

Whose devices does it build on?

Its devices cite 4 predicates; 1 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 4 times; 1 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.

  • K200717CLEWICU System (ClewICUServer and ClewICUnitor)Clew Medical, Ltd. · 20214cite it

What has FDA decided for it lately?

  • K233216CLEWICU SystemClew Medical, Ltd. · 2024
  • K200717CLEWICU System (ClewICUServer and ClewICUnitor)Clew Medical, Ltd. · 2021

All 2 as Clew Medical, Ltd. →