# Invia

> Medical device manufacturer record on deviCERTS, compiled from public registries. Invia is a medical device manufacturer based in the United States, with 8 devices listed in FDA GUDID, FDA 510(k) and EUDAMED (FDA Class II) as of 15 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/invia>
- Also registered as: INVIA, LLC
- Country: United States (from SRN)
- EUDAMED actor status: active
- Role: Manufacturer
- Registrations: EUDAMED
- EUDAMED SRN: US-MF-000008976

## Figures

- Devices: 8
- EU certificates: 1
- 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 5, FDA 510(k) 3, EUDAMED 1
- Device classes: FDA Class II 8

## Devices

The first 8 of 8, in the order of the canonical page, which lists them all.

- [4DM](https://devicerts.com/devices/4dm-qih) · ref K260879 · Class II · 510(k) · status: Active · decision 2026-09-10
- [Corridor4DM v2016](https://devicerts.com/devices/corridor4dm-v2016) · Class II · GUDID · status: Active
- [Corridor4DM v2017](https://devicerts.com/devices/corridor4dm-v2017) · Class II · GUDID · status: Active
- [Corridor4DM C4DM10](https://devicerts.com/devices/corridor4dm-c4dm10) · Class II · EUDAMED, GUDID · status: Active
- [Corridor4DM v2013](https://devicerts.com/devices/corridor4dm-v2013) · Class II · GUDID · status: Active
- [Corridor4DM v2015](https://devicerts.com/devices/corridor4dm-v2015) · Class II · GUDID · status: Active
- [CORRIDOR4DM](https://devicerts.com/devices/corridor4dm-kps) · ref K080575 · Class II · 510(k) · status: Active · decision 2008-05-13
- [CORRIDOR4DM V2010 Model: V2010](https://devicerts.com/devices/corridor4dm-v2010-model-v2010-llz) · ref K101279 · Class II · 510(k) · status: Active · decision 2010-08-04

## EU certificates

- US25/00000108 · Quality management system · MDR · notified body SGS Belgium NV · issued 2026-06-15 · expires 2030-03-18 · status: amended

## Source and citation

- Cite as: Invia. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/invia (data as of 2026-11-15).
- Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA GUDID](https://accessgudid.nlm.nih.gov/), [FDA 510(k)](https://open.fda.gov/apis/device/510k/)
- EUDAMED record synced: 2026-11-07
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-15
- JSON: <https://devicerts.com/manufacturers/invia.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/invia
- 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.