Data / Medical devices / United States / Invia, LLC
Invia, LLC: FDA-registered device maker in Ann Arbor, MI, United States, 1 510(k) clearance
Invia, LLC is registered with the FDA (registration 3004993756) in Ann Arbor, MI, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 4, 2010. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3004993756
- Address
- 8192 Jackson Rd, Ann Arbor, MI, United States, 48103
- Owner or operator
- INVIA, LLC (10023131)
- Roles
- Manufacturer
- First device listed
- November 21, 2013
- Registered through
- 2027
- Brand names listed
- Corridor4DM v2015, Corridor4DM v2016, Corridor4DM v2017, Corridor4DM v2018, Corridor4DM v2023, Corridor4DM v2024, Corridor4DM v2025
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Image Processing, Radiological | LLZ | 2 | Manufacturer | accessdata.fda.gov |
| System, Tomography, Computed, Emission | KPS | 2 | Manufacturer | accessdata.fda.gov |
| System, X-Ray, Tomography, Computed | JAK | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 4, 2010 | K101279 | CORRIDOR4DM V2010 MODEL: V2010 | LLZ | Substantially Equivalent | Invia | accessdata.fda.gov |
Compare with other makers
- All makers of System, Tomography, Computed, Emission
- All makers of System, Image Processing, Radiological
- All makers of System, X-Ray, Tomography, Computed
Updated August 4, 2010. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.