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Data / Medical devices / United States / MetriTrack, Inc.

MetriTrack, Inc.: FDA-registered device maker in Oak Brook, IL, United States, 1 510(k) clearance

MetriTrack, Inc. is registered with the FDA (registration 3011411309) in Oak Brook, IL, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 26, 2021. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3011411309
Address
1010 Jorie Blvd Ste 48, Oak Brook, IL, United States, 60523
Owner or operator
Metritrack, Inc. (10048313)
Roles
Complaint file establishment, Manufacturer
First device listed
February 6, 2023
Registered through
2026
Brand names listed
Breast Volume Navigator (BVN) Model G-2000

Devices it lists

DeviceProduct codeClassRoleSource
System, Image Processing, RadiologicalLLZ2Complaint file establishment, Manufactureraccessdata.fda.gov
System, Imaging, Pulsed Echo, UltrasonicIYO2Complaint 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
May 26, 2021K211098Breast Volume Navigator (BVN) Model G-2000IYOSubstantially EquivalentMetritrack, Inc.accessdata.fda.gov

Compare with other makers

Updated May 26, 2021. 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.