# Advalight Aps

> Medical device manufacturer record on deviCERTS, compiled from public registries. Advalight Aps is a medical device manufacturer, with 3 devices listed in FDA 510(k), EUDAMED and FDA GUDID (FDA Class II) as of 15 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/advalight-aps>
- Country: not established
- Role: Manufacturer
- DUNS: 310762054

## Figures

- Devices: 3
- FDA recalls (matched to the firm by name): 0
- Sites: 1

## Registry facts

*Every device of the manufacturer. A device listed in two registries counts in both.*

- Registries: FDA 510(k) 2, EUDAMED 1, FDA GUDID 1
- Device classes: FDA Class II 3

## Sites and related companies

- Site: [AdvaLight APS](https://devicerts.com/manufacturers/fda-fei-3010683226) (Denmark)

## Devices

The first 3 of 3, in the order of the canonical page, which lists them all.

- [ADVATx 1.0](https://devicerts.com/devices/advatx-684) · Class II · EUDAMED, GUDID · status: Active
- [AdvaTx](https://devicerts.com/devices/advatx-gex-k250189) · ref K250189 · Class II · 510(k) · status: Active · decision 2025-04-01
- [Advatx](https://devicerts.com/devices/advatx-gex) · ref K132976 · Class II · 510(k) · status: Active · decision 2014-04-17

## Source and citation

- Cite as: Advalight Aps. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/advalight-aps (data as of 2026-11-15).
- Data sources: [FDA 510(k)](https://open.fda.gov/apis/device/510k/), [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA GUDID](https://accessgudid.nlm.nih.gov/)
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-15
- JSON: <https://devicerts.com/manufacturers/advalight-aps.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/manufacturers/advalight-aps
- 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.