# pNeuton 58210

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

- Canonical page: <https://devicerts.com/devices/pneuton-58210>
- Manufacturer: [Airon Corporation](https://devicerts.com/manufacturers/airon-corporation) (United States, FDA 510(k) applicant)
- Device class: Class II (US FDA)
- FDA product code: CAH
- GMDN: Non-respiratory device ambient air filter (11711)

## Registrations and authorizations

- **GUDID** · GUDID listing · United States · UDI-DI 00853678006672 · listed 2017-01-10 · status: Listed (GUDID: in commercial distribution)
- **GUDID** · FDA 510(k) · United States · K925217 · decision 1993-01-26 · decision SESE · status: Active · from GUDID

## Recalls

- Z-0449-2026 · Class I · ongoing · initiated 2025-10-10: Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment.
- Z-3031-2024 · Class II · ongoing · initiated 2024-04-08: Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.

## Identity

- Trade name: pNeuton [FDA GUDID (AccessGUDID)]
- Generic name: Non-respiratory device ambient air filter [FDA GUDID (AccessGUDID)]
- Model / Ref / Catalog: 58210 [FDA GUDID (AccessGUDID)]

## Identifiers

- Primary DI / UDI-DI: 00853678006672 [FDA GUDID (AccessGUDID)]
- 510(k) Number: K925217 [FDA GUDID (AccessGUDID)]
- FDA product code: CAH [FDA GUDID (AccessGUDID)]
- GMDN term: Non-respiratory device ambient air filter (11711) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class II [FDA GUDID (AccessGUDID)]
- Regulation number: 868.5260 [FDA GUDID (AccessGUDID)]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Dimensions & Sizes

- Size: Weight — 0.04 Pound [FDA GUDID (AccessGUDID)]; Height — 2.50 Inch [FDA GUDID (AccessGUDID)]; Width — 2.50 Inch [FDA GUDID (AccessGUDID)]; Length — 2.75 Inch [FDA GUDID (AccessGUDID)]

## Properties

- Single use: Yes [FDA GUDID (AccessGUDID)]
- Prescription use: Yes [FDA GUDID (AccessGUDID)]
- Lot / batch number: Yes [FDA GUDID (AccessGUDID)]
- Expiration date: Yes [FDA GUDID (AccessGUDID)]
- Manufacturing date: Yes [FDA GUDID (AccessGUDID)]
- Supplied sterile: No [FDA GUDID (AccessGUDID)]
- Sterilise before use: No [FDA GUDID (AccessGUDID)]
- Implantable: No [FDA GUDID (AccessGUDID)]
- Contains latex: No [FDA GUDID (AccessGUDID)]
- Over-the-counter: No [FDA GUDID (AccessGUDID)]
- Convenience kit: No [FDA GUDID (AccessGUDID)]
- Combination product: No [FDA GUDID (AccessGUDID)]
- HCT/P: No [FDA GUDID (AccessGUDID)]
- Premarket exempt: No [FDA GUDID (AccessGUDID)]
- Serial number: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: pNeuton 58210, Airon Corporation. deviCERTS medical device catalogue. https://devicerts.com/devices/pneuton-58210 (data as of 2026-11-14).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/), [FDA recalls](https://open.fda.gov/apis/device/recall/)
- Registry records last synced: 2026-10-22
- Statuses computed as of: 2026-11-14
- JSON: <https://devicerts.com/devices/pneuton-58210.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/pneuton-58210
- 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.