CENTER FOR PAIN AND STRESS RESEARCH, LTD.

FDA Device Registration & Listing · TORONTO Ontario, CA · Registration 3002669614

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
3002669614
FEI Number
3002669614
Entity Name
CENTER FOR PAIN AND STRESS RESEARCH, LTD.
City/State/Country
TORONTO Ontario, CA
Establishment Address
3679A LAKESHORE BLVD WEST, TORONTO Ontario M8W 1P7, CA
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
CENTER FOR PAIN AND STRESS RESEARCH, LTD. (Owner Number: 9025652)
Owner / Operator Contact Address
3679 Lakeshore Blvd. W., --, TORONTO, CA-ON M8W 1P7, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Dolphin Neurostim Professional OTC Dolphin Neurostim OTC Dolphin Neurostim Dolphin Neurostim Professional

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter Neurology Class 2 882.5890 2017-10-18
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2003-06-23

Official Correspondent

No official correspondent registered.

US Agent Details

Richard Keen Business: Compliance Consultants Email: rkeen@fda-complianceconsultants.com Phone: (203) 3292700

Related Public Records

Same Entity

CENTER FOR PAIN AND STRESS RESEARCH, LTD.
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 3002669614. Last updated year: 2026. Please use registration number 3002669614 when referencing this establishment in official correspondence.
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