# Circassia AB

> Medical device manufacturer record on deviCERTS, compiled from public registries. Circassia AB is a medical device manufacturer, with 25 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II) as of 15 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/circassia-ab>
- Country: Sweden (FDA applicant, unverified)
- Role: Manufacturer
- DUNS: 632700860

## Figures

- Devices: 25
- FDA recalls (matched to the firm by name): 0

## Registry facts

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

- Registries: FDA GUDID 24, EUDAMED 4, FDA 510(k) 1
- Device classes: FDA Class II 25

## Devices

The first 25 of 25, in the order of the canonical page, which lists them all.

- [NIOX VERO Battery](https://devicerts.com/devices/niox-12-1150) · Class II · GUDID · status: Active
- [NIOX VERO Test Kit 300](https://devicerts.com/devices/niox-12-2830-us) · Class II · GUDID · status: Active
- [NIOX MINO Sensor 50](https://devicerts.com/devices/niox-03-2005) · Class II · GUDID · status: Active
- [NIOX VERO Filter](https://devicerts.com/devices/niox-12-1018) · Class II · GUDID · status: Active
- [NIOX VERO Sensor 60](https://devicerts.com/devices/niox-12-1606) · Class II · GUDID · status: Active
- [NIOX MINO Sensor 500](https://devicerts.com/devices/niox-03-2050) · Class II · GUDID · status: Active
- [NIOX VERO Starter Kit 300](https://devicerts.com/devices/niox-12-1830-us) · Class II · GUDID · status: Active
- [NIOX VERO Test Kit 500](https://devicerts.com/devices/niox-12-2850-us) · Class II · GUDID · status: Active
- [NIOX VERO Sensor 1000](https://devicerts.com/devices/niox-12-1700) · Class II · GUDID · status: Active
- [Niox Mino 09](https://devicerts.com/devices/niox-09-1100) · Class II · GUDID · status: Active
- [NIOX VERO Handle](https://devicerts.com/devices/niox-12-1010) · Class II · EUDAMED, GUDID · status: Active
- [NIOX Apps / Panel](https://devicerts.com/devices/niox-12-1004) · Class II · GUDID · status: Active
- [Niox Vero](https://devicerts.com/devices/niox-12-1000) · Class II · GUDID · status: Active
- [NIOX MINO Sensor 300](https://devicerts.com/devices/niox-03-2030) · Class II · GUDID · status: Active
- [NIOX VERO Test Kit 1000](https://devicerts.com/devices/niox-12-2900-us) · Class II · GUDID · status: Active
- [NIOX MINO Sensor 1000](https://devicerts.com/devices/niox-03-2100) · Class II · GUDID · status: Active
- [NIOX MINO NO Scrubber](https://devicerts.com/devices/niox-09-1300) · Class II · GUDID · status: Active
- [NIOX MINO Sensor 100](https://devicerts.com/devices/niox-03-2010) · Class II · GUDID · status: Active
- [NIOX VERO Sensor 500](https://devicerts.com/devices/niox-12-1650) · Class II · EUDAMED, GUDID · status: Active
- [NIOX VERO Sensor 300](https://devicerts.com/devices/niox-12-1630) · Class II · EUDAMED, GUDID · status: Active
- [NIOX VERO Starter Kit 100](https://devicerts.com/devices/niox-12-1810-us) · Class II · GUDID · status: Active
- [NIOX VERO Test Kit 100](https://devicerts.com/devices/niox-12-2810-us) · Class II · GUDID · status: Active
- [NIOX MINO Filter](https://devicerts.com/devices/niox-02-1201) · Class II · GUDID · status: Active
- [NIOX VERO Sensor 100](https://devicerts.com/devices/niox-12-1610) · Class II · EUDAMED, GUDID · status: Active
- [Niox Vero](https://devicerts.com/devices/niox-vero-mxa) · ref K170983 · Class II · 510(k) · status: Active · decision 2017-11-22

## Source and citation

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