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Data / Medical devices / United States / Ultragreen Data Systems Inc.

Ultragreen Data Systems Inc.: FDA-registered device maker in Long Island City, NY, United States, 1 510(k) clearance

Ultragreen Data Systems Inc. is registered with the FDA (registration 3040602603) in Long Island City, NY, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 17, 2015. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3040602603
Address
25-01 Jackson Avenue Suite 1810, Long Island City, NY, United States, 11101
Owner or operator
UltraGreen Data Systems Inc. (10094013)
Roles
Complaint file establishment, Manufacturer
First device listed
September 11, 2025
Registered through
2026
Brand names listed
Diagnostic Green, UltraLinq, UpLinq

Devices it lists

DeviceProduct codeClassRoleSource
System, Image Processing, RadiologicalLLZ2Complaint file establishment, Manufactureraccessdata.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
July 17, 2015K143176UltraLinqLLZSubstantially EquivalentUltralinq Healthcare Solutions, Inc.accessdata.fda.gov

Compare with other makers

Updated July 17, 2015. 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.