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Data / Medical devices / United States / Jointvue, LLC

Jointvue, LLC: FDA-registered device maker in Knoxville, TN, United States, 2 510(k) clearances

Jointvue, LLC is registered with the FDA (registration 3013535906) in Knoxville, TN, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 25, 2021. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3013535906
Address
2450 E.J. Chapman Drive Suite 104A, Knoxville, TN, United States, 37996
Owner or operator
JointVue, LLC (10055889)
Roles
Manufacturer
First device listed
November 27, 2017
Registered through
2026
Brand names listed
3D Echo, jFit

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
June 25, 2021K2116563D Echo v1.1LLZSubstantially EquivalentJointvue, LLCaccessdata.fda.gov
November 15, 2017K173329jFit Surgical PlannerLLZSubstantially EquivalentJointvue, LLCaccessdata.fda.gov

Compare with other makers

Updated June 25, 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.