# Wizair Compression System

> Active: United States. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/wizair-compression-system-jow>
- Manufacturer: [Medical Compression Systems (Dbn), Ltd.](https://devicerts.com/manufacturers/medical-compression-systems-dbn-ltd) (Israel, FDA 510(k) applicant)
- Name in the registry: WIZAIR COMPRESSION SYSTEM
- Device class: Class II (US FDA)
- FDA product code: JOW

## Overview

The WIZAIR COMPRESSION SYSTEM is a groundbreaking cardiovascular compression device that has been substantially equivalent to the ISO 11613-1 standard for over two decades. Our device has undergone rigorous testing and has been certified by regulatory authorities around the world, ensuring its safety and efficacy. With its advanced technology and user-friendly design, this device is an ideal solution for medical professionals looking to provide high-quality compression therapy.

## Registrations and authorizations

- **510(k)** · FDA 510(k) · United States · K023573 · decision 2002-11-21 · decision SESE · status: Active

## Recalls

- Z-0387-2012 ·  · terminated · initiated 2011-08-28: This voluntary field action is being undertaken because MCS has received a limited number of reports involving the use of a non-MCS AC/DC adaptor with the ActiveCare DVT and ActiveCare+S.F.T. devices. The firm found that an ActiveCare DVT device may work improperly if connected to a non-MCS AC/DC adaptor with a higher nominal voltage. As specified in each product's User Manual, the ActiveCare DVT

## Identifiers

- 510(k) Number: K023573 [FDA 510(k)]
- FDA product code: JOW [FDA 510(k)]

## Classification

- Device class: Class II [FDA 510(k)]
- Regulation: 21 CFR Part 870.5800 [FDA 510(k)]
- Advisory committee: Cardiovascular [FDA 510(k)]
- FDA decision: SESE [FDA 510(k)]

## Source and citation

- Cite as: Wizair Compression System, Medical Compression Systems (Dbn), Ltd. deviCERTS medical device catalogue. https://devicerts.com/devices/wizair-compression-system-jow (data as of 2026-11-15).
- Data sources: [FDA 510(k)](https://open.fda.gov/apis/device/510k/), [FDA recalls](https://open.fda.gov/apis/device/recall/)
- Registry records last synced: 2026-10-22
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/wizair-compression-system-jow.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/devices/wizair-compression-system-jow
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.