TRUERELIEF

FDA Device Registration & Listing · Santa Monica, CA, US · Registration 3015550326

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3015550326
FEI Number
3015550326
Entity Name
TRUERELIEF
City/State/Country
Santa Monica, CA, US
Establishment Address
100 Wilshire Boulevard, Suite 700, Santa Monica, CA 90401, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
TrueRelief (Owner Number: 10060510)
Owner / Operator Contact Address
100 Wilshire Boulevard, Suite 700, Santa Monica, CA 90401, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K202186
PMA Number
N/A

All Registered Proprietary Names

TRUERELIEF, Model 1250 TRUERELIEF Device, TRUERELIEF 1250 TRUERELIEF Kit, Model TR1250C TRUERELIEF Kit TRUERELIEF Secondary Probe, Model P12S Secondary Probe TRUERELIEF Power Cord with Wall Wart, Model WW12 Power Cord with Wall Wart TRUERELIEF Primary Probe, Model P12P Primary Probe TRUERELIEF Probe Tips, Probe Tips, Model P12T10 Probe Tips TrueRellief Device

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2019-05-20
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2021-08-10

Official Correspondent

John Crosson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TrueRelief
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K122948 Gemore Technology Co, Ltd. GEM-STIM COMBO STIMULATOR 2012-12-21
K033455 Biomedical Life Systems, Inc. ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS03-5 2004-01-15
K810593 Medical Devices, Inc. NEUROPAC ULTRA I 1981-03-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015550326. Last updated year: 2026. Please use registration number 3015550326 when referencing this establishment in official correspondence.
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