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RelieVRx RVX-3002

by Appliedvr United States GUDID

Product code QRA

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850038247140 UDI-DIDate20 Nov 2025ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls: none on record (FDA, checked 22 Oct 2026)

Specification

GUDID · synced 22 Oct 2026

Trade Name
RelieVRx
Generic Name
Pain relief virtual reality system
Model / Reference
RVX-3002
Primary DI / UDI-DI
00850038247140
510(k) Number
FDA Product Code
QRA
GMDN Term
Pain relief virtual reality system
Device Class
Class II
Regulation Number
890.5800
Commercial Distribution
In Commercial Distribution

Other devices from Appliedvr

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Properties & raw data

Show properties, registry sources and raw records
  • Prescription Use
  • Serial Number
Other properties (12)
  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No

Sources (1)

  • FDA UDI d4ecc46b-19f1-4199-a7a8-cefd4098a01f 35 fields · synced 22 Oct 2026