# ZIIP+ Device

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

- Canonical page: <https://devicerts.com/devices/ziip-device-nfo-k212342>
- Manufacturer: [Ziip, Inc.](https://devicerts.com/manufacturers/ziip-llc) (United States, FDA 510(k) applicant)
- Device class: Class II (US FDA)
- FDA product code: NFO

## Overview

The ZIIP+ Device is a high-quality, FDA-cleared neurostimulator designed for the treatment of various neurological conditions. This device uses transcutaneous electrical stimulation to modulate neural activity, providing effective pain relief and improving quality of life for patients.

## Registrations and authorizations

- **510(k)** · FDA 510(k) · United States · K212342 · decision 2021-09-23 · decision SESE · status: Active

## Recalls

No recall on record.

## Identifiers

- 510(k) Number: K212342 [FDA 510(k)]
- FDA product code: NFO [FDA 510(k)]

## Classification

- Device class: Class II [FDA 510(k)]
- Regulation: 21 CFR Part 882.5890 [FDA 510(k)]
- Advisory committee: Neurology [FDA 510(k)]
- FDA decision: SESE [FDA 510(k)]

## Source and citation

- Cite as: ZIIP+ Device, Ziip, Inc. deviCERTS medical device catalogue. https://devicerts.com/devices/ziip-device-nfo-k212342 (data as of 2026-11-15).
- Data sources: [FDA 510(k)](https://open.fda.gov/apis/device/510k/)
- Registry records last synced: 2026-10-22
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/ziip-device-nfo-k212342.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/ziip-device-nfo-k212342
- 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.