510(k) Report

FDA applicant

Ahava Stein

Ginot Shomron, 44853, IL1 decision2001–20010 recalls

FDA records 1 decision for Ahava Stein (Ginot Shomron, 44853, IL) in 2001: 1 510(k) clearance. All are in product code IRP (Massager, Powered Inflatable Tube). 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, physical medicine panel, where it files most

How often FDA has decided Ahava Stein’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ahava Stein since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ahava Stein 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?

  • IRPMassager, Powered Inflatable Tube1decision

Who builds on its devices?

Later devices cite its devices 2 times; 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.

  • K000655Ppcid- Pneumatic Peripheral Circulation Improvement (Footrest) DeviceAhava Stein · 20012cite it

What has FDA decided for it lately?

  • K000655Ppcid- Pneumatic Peripheral Circulation Improvement (Footrest) DeviceAhava Stein · 2001

The one decision as Ahava Stein →