Appliedvr

Van Nuys, CA, US

APPLIEDVR appears in FDA device records in Van Nuys, CA. FDA records list 3 510(k) clearances between 2021-11-16 and 2025-08-13, no PMA records and one registered establishment. As of 2026-09-10, FDA records show one recall for this company, and at least one establishment registration is current.

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

510(k) clearance history

FDA records hold 3 510(k) clearances for Appliedvr between 2021 and 2025. The busiest year on record is 2021, with 1. The most recent is 2025, with 1.

Clearances by year, as a table

510(k) clearance decisions for Appliedvr, by decision year
Year	Clearances
2021	1
2024	1
2025	1

510(k) clearances on record, most recent first
K number	Device	Product code	Decision	Decision date
K251519	RelieVRx (Pico G3)	QRA	Substantially Equivalent	2025-08-13
K243417	RelieVRx	QRA	Substantially Equivalent	2024-12-04
DEN210014	EaseVRx	QRA	Unknown	2021-11-16

Registered establishments

FDA registered establishments for Appliedvr, with the product codes listed at each
Registration	FEI	Establishment	Address	Registration expires	Product codes listed
3021071568	3021071568	APPLIEDVR	16760 Stagg St Unit 216, Van Nuys, CA 91406 US	2026	QRA

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

FDA product codes

QRAVirtual Reality Behavioral Therapy Device For Pain Relief

Recall records

Device recall records naming this company, most recent first
Recall	Product	Reason	Classification	Initiated	Status
Z-2044-2023	RelieVR REF: RVX-2002, Rx Only. Virtual reality behavioral therapy device for pain relief.	There is the potential for the program software to malfunction which will not allow it to move forward to the next session.	Class II	2023-02-27	Completed

Verification record

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