Invia
Active in EUDAMEDUnited Statesfrom SRN EUDAMED SRN US-MF-000008976
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.
- Devices
- 8
- Registrations
- EUDAMED
Registry facts
- Registries
- FDA GUDID 5
- FDA 510(k) 3
- EUDAMED 1
- Device classes
- FDA Class II 8
- Identifiers
- EUDAMED SRN US-MF-000008976
At a glance
EU certificates
1 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
What Invia makes
Invia develops DICOM-compatible image processing software designed for radiology workflows, enabling integration and analysis of medical imaging data across hospital systems. The Corridor4DM platform supports multi-dimensional imaging data management, including time-series and volumetric datasets, to enhance diagnostic and research applications.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) databases. Invia is headquartered in the United States.
Catalogue
4DM Ref K260879
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: CE MDR CE MDD 510(k) Registry: EUDAMEDGUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
CORRIDOR4DM Ref K080575
Regimes: 510(k) Registry: 510(k)CORRIDOR4DM V2010 Model: V2010 Ref K101279
Regimes: 510(k) Registry: 510(k)
Company details
- EUDAMED SRN
- US-MF-000008976
- EUDAMED status
- Active
- EUDAMED registered name
- INVIA
- EUDAMED abbreviated name
- INVIA
- Registered address
- 8192, Jackson Road, 48103, Ann Arbor, United States
- Website
- www.inviasolutions.com
- Phone
- +01 734 205 1231
- PRRC contact
- Edward Ficaro
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 18 Mar 2030
SGS Belgium NV 1639 1 certificate
- US25/00000108 Active
Quality management system EU MDR
- Issued
- 15 Jun 2026
- Expires
- 18 Mar 2030
- Reason
- Mnf data change
Frequently asked questions
How many devices does Invia have in the registry?
The registry currently lists 8 devices for Invia. Devices recorded under merged duplicate company entries are counted once.
Which registries list Invia's devices?
Among its 8 most recently registered devices, Invia has devices listed in EUDAMED (1 device), FDA 510(k) (3 devices) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Invia's devices fall under?
Among its 8 most recently registered devices, the classes recorded for Invia's devices are Class II. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Invia?
EUDAMED lists 1 certificate for Invia (quality management system) under MDR. The most recent was issued on 15 Jun 2026.
What are the newest devices from Invia in the registry?
The most recently registered devices listed for Invia include 4DM, Corridor4DM v2016, Corridor4DM v2017 and Corridor4DM C4DM10.