FDA.reportPublic FDA data

APPLIEDVR

Matched from indexed company URL: Appliedvr

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30210715683021071568APPLIEDVR1N2026-01-0116760 Stagg St Unit 216 Van Nuys CA US 91406

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00850038247102RelieVRx - RelieVRx is an at-home immersive virtual reality (VR) pain treatment indicated as adjunctive treatment for chronic lower back pain (CLBP).(844) 728-4487Support@AVRPathway.com
00850038247119RelieVRx - RelieVRx is an at-home immersive virtual reality (VR) pain treatment indicated as adjunctive treatment for chronic lower back pain (CLBP).(844) 728-4487Support@AVRPathway.com
00850038247126RelieVRx - RelieVRx is an at-home immersive virtual reality (VR) pain treatment indicated as adjunctive treatment for chronic lower back pain (CLBP).(844) 728-4487Support@AVRPathway.com
00850038247133RelieVRx - RelieVRx is an at-home immersive virtual reality (VR) pain treatment indicated as adjunctive treatment for chronic lower back pain (CLBP).(844) 728-4487Support@AVRPathway.com
00850038247140RelieVRx - RelieVRx is an at-home immersive virtual reality (VR) pain treatment indicated as adjunctive treatment for chronic lower back pain (CLBP).(844) 728-4487Support@AVRPathway.com
00850038247157RelieVRx - RelieVRx is an at-home immersive virtual reality (VR) pain treatment indicated as adjunctive treatment for chronic lower back pain (CLBP).(844) 728-4487Support@AVRPathway.com
00850038247164RelieVRx - RelieVRx is an at-home immersive virtual reality (VR) pain treatment indicated as adjunctive treatment for chronic lower back pain (CLBP).(844) 728-4487Support@AVRPathway.com
00850038247171RelieVRx - RelieVRx is an at-home immersive virtual reality (VR) pain treatment indicated as adjunctive treatment for chronic lower back pain (CLBP).(844) 728-4487Support@AVRPathway.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2997341736799771K243417RelieVRxQRA2024-12-04
2997341477700699DEN210014EaseVRxQRA2021-11-16

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
QRA22024-12-04

PMN#

GUDID#