FDA applicant

Mego Afek

Kfar Saba, IL6 decisions1981–20260 recalls

FDA records 6 decisions for Mego Afek (Kfar Saba, IL) from 1981 to 2026: 6 510(k) clearances. Most are in product codes JOW (Sleeve, Limb, Compressible) and IRP (Massager, Powered Inflatable Tube). Its devices cite 5 predicates, 2 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Mego Afek , Ltd.”.

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 Mego Afek’s devices, and how often a recall has named them.

FDA decisions per year

1in 2023

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mego Afek’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) Report

Other applicant names beginning “Mego”

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

Mego Afek AC, Ltd. 17

Mego Afek

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Mego”