REMINGTON MEDICAL

FDA Device Registration & Listing · Markham Ontario, CA · Registration 3001676837

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
3001676837
FEI Number
3001676837
Entity Name
REMINGTON MEDICAL
City/State/Country
Markham Ontario, CA
Establishment Address
401 Bentley St, Suite 9, Markham Ontario L3R9T2, CA
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Remington Medical (Owner Number: 10052253)
Owner / Operator Contact Address
401 Bentley St, Suite 9, Markham, CA-ON L3R9T2, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K203710
PMA Number
N/A

All Registered Proprietary Names

D-ACTOR® 200 Vibration Massage System D-ACTOR 100 Vibration Massage System D-ACTOR 50 Vibration Massage System Magnetolith

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2016-07-06
NGX Stimulator, Muscle, Powered, For Muscle Conditioning Physical Medicine Class 2 890.5850 2023-09-19
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2023-09-19

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Remington Medical
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
K221200 Xbody Hungary Kft. XBody Go USA, XBody Pro USA 2023-01-31
K030403 Cefar Medical AB CEFAR REHAB 2 AND REHAB 2 PRO 2003-07-17
K231440 Shenzhen Roundwhale Technology Co. , Ltd. Combo Electrotherapy Device 2023-11-03
K820884 Nitron Electronics ELECTRICAL MUSCLE STIMULATOR 1982-04-29
K201958 Therasigma, LLC ETD Family of Electrotherapy Devices 2020-08-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3001676837. Last updated year: 2026. Please use registration number 3001676837 when referencing this establishment in official correspondence.
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