Data / Medical devices / Canada / Remington Medical
Remington Medical: FDA-registered device maker in Markham Ontario, Canada, 2 510(k) clearances
Remington Medical is registered with the FDA (registration 3001676837) in Markham Ontario, Canada. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 3, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3001676837
- Address
- 401 Bentley St Suite 9, Markham Ontario, Canada, L3R9T2
- Owner or operator
- Remington Medical (10052253)
- Roles
- Exporter to the US
- First device listed
- July 6, 2016
- Registered through
- 2026
- Brand names listed
- D-ACTOR 100 Vibration Massage System, D-ACTOR 50 Vibration Massage System, D-ACTOR® 200 Vibration Massage System, Magnetolith
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Massager, Therapeutic, Electric | ISA | 1 | Exporter to the US | accessdata.fda.gov |
| Stimulator, Muscle, Powered | IPF | 2 | Exporter to the US | accessdata.fda.gov |
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 3, 2021 | K203710 | Storz Medical MAGNETOLITH Muscle Stimulator | IPF | Substantially Equivalent | Storz Medical AG | accessdata.fda.gov |
| August 30, 2001 | K002908 | JET THERAPY | ISA | Substantially Equivalent | Jet Therapy | accessdata.fda.gov |
Compare with other makers
- All makers of Massager, Therapeutic, Electric
- All makers of Stimulator, Muscle, Powered, For Muscle Conditioning
- All makers of Stimulator, Muscle, Powered
Updated May 3, 2021. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.