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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

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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
August 4, 2010K101279CORRIDOR4DM V2010 MODEL: V2010LLZSubstantially EquivalentInviaaccessdata.fda.gov

Compare with other makers

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.