510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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DEN210014Unknown

EaseVRx

Appliedvr, Van Nuys CA / Direct, Unknown
FDA source (opens on fda.gov)

DEN210014 is the FDA 510(k) clearance record for EaseVRx, a class II device, cleared for Appliedvr, Inc. on under FDA product code QRA (Virtual Reality Behavioral Therapy Device For Pain Relief). FDA's definition for product code QRA reads: "A virtual reality behavioral therapy device for pain relief is a device intended to provide behavioral therapy for patients with pain. Therapy is administered via a virtual reality display which utilizes a software program containing the...". FDA records list 3 510(k) clearances for Appliedvr, Inc., from to . As of , FDA records show no recalls naming DEN210014.

Clearance record

Decision date
Received
(231 days to decision)
Product code
QRA Virtual Reality Behavioral Therapy Device For Pain Relief
Regulation
21 CFR 890.5800
Device class
Class II
Review panel
Neurology
Applicant
Appliedvr, Inc. 16760 Stagg St., Suite 216, Van Nuys CA
Third party review
No

Clearances, product code QRA

Trailing 12 months
1 clearance under product code QRA in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code QRA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260