Jointvue, LLC

Knoxville, TN, US

JOINTVUE, LLC appears in FDA device records in Knoxville, TN. FDA records list 3 510(k) clearances between 2017-09-14 and 2021-06-25, no PMA records and one registered establishment. As of 2026-09-10, FDA records show no recalls for this company, and at least one establishment registration is current.

510(k) clearances: 3
PMA records: 0
Recall records: 0
Registered establishments: 1

510(k) clearance history

FDA records hold 3 510(k) clearances for Jointvue, LLC between 2017 and 2021. The busiest year on record is 2017, with 2. The most recent is 2021, with 1.

Clearances by year, as a table

510(k) clearance decisions for Jointvue, LLC, by decision year
Year	Clearances
2017	2
2021	1

510(k) clearances on record, most recent first
K number	Device	Product code	Decision	Decision date
K211656	3D Echo v1.1	LLZ	Substantially Equivalent	2021-06-25
K173329	jFit Surgical Planner	LLZ	Substantially Equivalent	2017-11-15
K172513	3D Echo	LLZ	Substantially Equivalent	2017-09-14

Registered establishments

FDA registered establishments for Jointvue, LLC, with the product codes listed at each
Registration	FEI	Establishment	Address	Registration expires	Product codes listed
3013535906	3013535906	JOINTVUE, LLC	2450 E.J. Chapman Drive, Knoxville, TN 37996 US	2026	IYO LLZ

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of 2026-09-28, FDA export datePage updated 2026-09-05Source: openFDA, public domain