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Data / Medical devices / United States / Luminoah

Luminoah: FDA-registered device maker in Charlottesville, VA, United States, 1 510(k) clearance

Luminoah is registered with the FDA (registration 3046434077) in Charlottesville, VA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 20, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3046434077
Address
1 Morton Dr Ste 100, Charlottesville, VA, United States, 22903
Owner or operator
Luminoah (10096019)
Roles
Complaint file establishment, Manufacturer, Specification developer
First device listed
June 9, 2026
Registered through
2026
Brand names listed
Luminoah Flow Enteral Feeding Pump, Luminoah Flow Enteral Nutrition Delivery System, Luminoah Flow Enteral Nutrition System, Luminoah Flow Enteral Pump, Luminoah Flow Enteral System

Devices it lists

DeviceProduct codeClassRoleSource
Pump, Infusion, EnteralLZH2Complaint file establishment, Manufacturer, Specification developeraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
April 20, 2026K253558Luminoah FLOW™ Enteral Nutrition SystemLZHSubstantially EquivalentLuminoahaccessdata.fda.gov

Compare with other makers

Updated April 20, 2026. 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.