FDA applicant

Iren-Medical, Ltd.

Or Aquiva, IL1 decision2022–20220 recalls

FDA records 1 decision for Iren-Medical, Ltd. (Or Aquiva, IL) in 2022: 1 510(k) clearance. All are in product code FKX (System, Peritoneal, Automatic Delivery). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

1in 2022

2022high 1 (2022) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Iren-Medical, Ltd. by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Iren-Medical, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?