# Accufit

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

- Canonical page: <https://devicerts.com/devices/accufit-ipf>
- Manufacturer: [Mettler Electronics Corporation](https://devicerts.com/manufacturers/fda-fei-2013558) (FDA registration: United States)
- Name in the registry: accufit
- Device class: Class II (US FDA)
- FDA product code: IPF

## Overview

*AI-generated summary, 2026-10-01. Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data is the record.*

The Accufit is a Physical Medicine Device (Product Code IPF) designed for muscle reeducation and stimulation therapy. It delivers electrical impulses to facilitate neuromuscular recovery, aiding in rehabilitation and pain management. The device incorporates two waveform configurations derived from a predecessor model, ensuring compatibility with established therapeutic protocols. Its classification as a Class 2 device reflects its role in controlled, evidence-based clinical applications.

The Accufit is supplied as a reusable medical device, intended for use in clinical settings such as physical therapy or rehabilitation centers. It is not described as sterile or single-use, and no MRI safety information is provided in the regulatory data. The device was cleared via the Traditional 510(k) pathway (K223802) under the FDA’s Physical Medicine advisory committee, with a decision date of October 6, 2023. No additional regulatory markings (e.g., CE) or third-party certifications are mentioned in the available documentation.

## Registrations and authorizations

- **510(k)** · FDA 510(k) · United States · K223802 · decision 2023-10-06 · decision SESE · status: Active

## Recalls

No recall on record.

## Identifiers

- 510(k) Number: K223802 [FDA 510(k)]
- FDA product code: IPF [FDA 510(k)]

## Classification

- Device class: Class II [FDA 510(k)]
- Regulation: 21 CFR Part 890.5850 [FDA 510(k)]
- Advisory committee: Physical Medicine [FDA 510(k)]
- FDA decision: SESE [FDA 510(k)]

## Source and citation

- Cite as: Accufit, Mettler Electronics Corporation. deviCERTS medical device catalogue. https://devicerts.com/devices/accufit-ipf (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/accufit-ipf.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/accufit-ipf
- 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.